SINthetic Pharmaceutical = ‘Poison of the Witch’ The Word ...
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SINthetic Pharmaceutical = ‘Poison of the Witch’ 1 The Word Pharmacy is from the Greek ‘The Poison of a Witch’
Transcript of SINthetic Pharmaceutical = ‘Poison of the Witch’ The Word ...
SINthetic Pharmaceutical = ‘Poison of the Witch’
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The Word Pharmacy is from the
Greek ‘The Poison of a Witch’
SINthetic Pharmaceutical = ‘Poison of the Witch’
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When a large percentage of the drugs once approved for sale need to be removed for hurting people, We must see that there is
something extremely wrong with the Approval process. What is wrong is that
SINthetic Patented PHARMACeuticals are trully the ‘Poison of the Witch’.
SINthetic Pharmaceutical = ‘Poison of the Witch’
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This Book will list some of these removed
drugs and explain the danger.
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This is a list of the Major drugs once approved for use now recalled a dangerous
Oxyphenisatin (Phenisatin) Australia, France,
Germany, UK, US Hepatotoxicity.[3]
Secobarbital France, Norway, others. Self poisoning.[3]
Lysergic acid
diethylamide (LSD)
1950
s–
1960
s
Marketed as a psychiatric
drug; withdrawn after it
became widely used
recreationally. Now illegal in
most of the world.
Thenalidine 1960 Canada, UK, US Neutropenia[3][53]
Thalidomide 1961 Germany
Withdrawn because of risk
of teratogenicity;[52] returned
to market for use
in leprosy and multiple
myeloma under FDAorphan
drug rules
Triparanol 1962 France, US Cataracts, alopecia,
ichthyosis.[3]
Bunamiodyl 1963 Canada, UK, US Nephropathy.[9]
Dantron 1963 Canada, UK, US
Genotoxicity.[13] withdrawn
from general use in UK but
permitted in terminal patients
SINthetic Pharmaceutical = ‘Poison of the Witch’
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Ethyl carbamate 1963 Canada, UK, US, Carcinogenicity.[20]
Benziodarone 1964 France, UK Jaundice.[3]
Butamben (Efocaine)(Butoform
e) 1964 US
Dermatologic toxicity;
psychiatric Reactions.[3]
Dithiazanine iodide 1964 France, US Cardiovascular and
metabolic reaction.[3]
Iodinated casein strophantin 1964 US Metabolic reaction.[3]
Iproniazid 1964 Canada
Interactions with food
products containing
tyrosine.[22]
Metofoline 1965 US Unspecific experimental
toxicity.[3]
Pronethalol 1965 UK Animal carcinogenicity.[3]
Xenazoic acid 1965 France Hepatotoxicity.[3]
Phenoxypropazine 1966 UK Hepatotoxicity, drug
intereaction.[3]
Bithionol 1967 US Dermatologic toxicity.[3]
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Ibufenac 1968 UK Hepatotoxicity, jaundice.[3]
Anagestone acetate 1969 Germany Animal carcinogenicity.[3]
Chlorphentermine 1969 Germany Cardiovascular Toxicity.[3]
Cloforex 1969 Germany Cardiovascular toxicity.[3]
Amoproxan 1970 France Dermatologic and ophthalmic
toxicity.[3]
Chlormadinone(Chlormenadion
e) 1970 UK, US Animal Carcinogenicity.[3]
Diethylstilbestrol
1970
s
Risk of teratogenicity[citation
needed]
Dihydrostreptomycin 1970 US Neuropsychiatric reaction.[3]
Fenclozic acid 1970 UK, US Jaundice, elevated hepatic
enzymes.[3]
Diacetoxydiphenolisatin 1971 Australia Hepatotoxicity.[3]
Triacetyldiphenolisatin 1971 Australia Hepatotoxicity.[3]
Dimazole (Diamthazole) 1972 France, US Neuropsychiatric reaction.[3]
SINthetic Pharmaceutical = ‘Poison of the Witch’
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Clioquinol 1973 France, Germany, UK,
US Neurotoxicity.[3]
Nialamide 1974 UK, US Hepatotoxicity, drug
intereaction.[3]
Dipyrone(Metamizole) 1975 UK, US, Others Agranulocytosis,
anaphylactic reactions.[3]
Mebanazine 1975 UK Hepatotoxicity, drug
intereaction.[3]
Phenacetin 1975 Canada
An ingredient in "A.P.C."
tablet; withdrawn because of
risk of cancer and kidney
disease[32] Germany
Denmark, UK, US, others
Reason: nephropathy.[3]
Azaribine 1976 US Thromboembolism.[3]
Oxeladin 1976 Canada, UK, US (1976) Carcinogenicity.[29]
Pifoxime (=Pixifenide) 1976 France Neuropsychiatric reaction.[3]
Phenformin and Buformin 1977 France, Germany US Severe lactic acidosis[3]
Buformin 1978 Germany Metabolic toxicity.[3]
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Alclofenac 1979 UK Vasculitis, Rash.[3]
Methapyrilene 1979 Germany, UK, US Animal carcinogenicity.[3]
Pyrovalerone 1979 France Abuse.[3]
Amobarbital 1980 Norway Self poisoning.[3]
Cyclobarbital 1980 Norway Self poisoning.[3]
Pentobarbital 1980 Norway Self poisoning.[3]
Ticrynafen(Tienilic acid) 1980 Germany, France, UK,
US others Liver toxicity and death.[3]
Nomifensine
1981
-
1986
France, Germany, Spain,
UK, US, others
Hemolytic Anemia,
hepatotoxicity, serious
hypersensitive reactions.[2][3]
Benoxaprofen 1982 Germany,Spain, UK, US
Liver and kidney failure;
gastrointestinal bleeding;
ulcers.[2][3]
Clomacron 1982 UK Hepatotoxicity.[3]
Methandrostenolone 1982 France, Germany, UK,
US, others Off-label abuse.[3]
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Pentylenetetrazol 1982
Withdrawn for inability to
produce effective convulsive
therapy, and for causing
seizures.
Dimethylamylamine (DMAA) 1983 US
Voluntarily withdrawn from
market by
Lily.[15]:12Reintroduced as
a dietary supplement in
2006;[15]:13 and in 2013 the
FDA started work to ban it
due to cardiovascular
problems[16]
Indoprofen 1983 Germany, Spain, UK Animal carcinogenicity,
gastrointestinal toxicity.[3]
Isoxicam 1983 France, Germany, Spain,
others Stevens johnson syndrome.[3]
Propanidid 1983 UK Allergy.[3]
Zimelidine 1983 Worldwide
Risk of Guillain-Barré
syndrome, hypersensitivity
reaction,
hepatotoxicity[3][57][58] banned
worldwide.[59]
Zomepirac 1983 UK, Germany, Spain, US
Anaphylactic reactions and
non-fatal allergic reactions,
renal failure[2][3]
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Althesin (=Alphaxoloneaminept
ine + Alphadolone) 1984 France, Germany, UK Anaphylaxis.[3]
Antrafenine 1984 France Unspecific experimental
toxicity.[3]
Fenclofenac 1984 UK Cutaneous reactions; animal
carcinogenicity.[3]
Feprazone 1984 Germany, UK Cutaneous reaction,
multiorgan toxicity.[3]
Glafenine 1984 France, Germany Anaphylaxis.[3]
Isaxonine phosphate 1984 France Hepatotoxicity.[3]
Methaqualone 1984
South Africa (1971), India
(1984), United Nations
(1971-1988)
Withdrawn because of risk
of addiction and overdose[26][2
7]
Nitrefazole 1984 Germany Hepatic and hematologic
toxicity.[3]
Oxyphenbutazone
1984
-
1985
UK, US, Germany,
France, Canada
Bone marrow suppression,
Steven Johnson
Syndrome.[3][30]
Cianidanol 1985 France, Germany, Spain,
Sweden Hemolytic Anemia.[3]
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Indalpine 1985 France Agranulocytosis.[3]
Perhexilene 1985 UK, Spain Neurologic and hepatic
toxicity.[3]
Phenylbutazone 1985 Germany Off-label abuse, hematologic
toxicity.[3]
Suloctidyl 1985 Germany, France, Spain Hepatotoxicity.[3]
Beta-ethoxy-lacetanilanide 1986 Germany Renal toxicity, animal
carcinogenicity.[3]
Bucetin 1986 Germany Renal toxicity.[3]
Canrenone 1986 Germany Animal Carcinogenicity.[3]
Difemerine 1986 Germany Multi-Organ toxicities.[3]
Sulfamethoxypyridazine 1986 UK Dermatologic and
hematologic reactions.[3]
Suprofen
1986
-
1987
UK, Spain, US Flank pain, decreased kidney
function.[2][3]
Clometacin 1987 France Hepatotoxicity.[3]
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Cyclofenil 1987 France Hepatotoxicity.[3]
Muzolimine 1987
France,
Germany,European
Union
Polyneuropathy.[3]
Vincamine 1987 Germany Hematologic toxicity.[3]
Cinepazide 1988 Spain Agranulocytosis.[10][11]
Nikethamide 1988 multiple markets CNS Stimulation.[3]
Prenylamine 1988 Canada,France,
Germany, UK, US, others
Cardiac arrythmia[37] and
death.[3]
Sulfacarbamide 1988 Germany Dermatologic, hematologic
and hepatic reactions .[3]
Sulfamethoxydiazine 1988 Germany Unknown.[3]
Broazolam 1989 UK Animal carcinogenicity.[3]
Etretinate 1989 France Withdrawn US (1999). Risk
for birth defects.[2][3]
Exifone 1989 France Hepatotoxicity.[3]
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L-tryptophan 1989 Germany, UK
Eosinophilic myalgia
syndrome.[3] Still sold in the
US
Proglumide 1989 Germany Respiratory reaction.[3]
Dilevalol 1990 UK Hepatotoxicity.[3]
Dinoprostone 1990 UK Uterine hypotonus, fetal
distress.[3]
Fenoterol 1990 New Zealand Asthma mortality.[3]
Metipranolol 1990 UK, others Uveitis.[3]
Pirprofen 1990 France, Germany, Spain Liver toxicity.[3][36]:223
Encainide 1991 UK, US Ventricular arrhythmias.[2][3]
Fipexide 1991 France Hepatotoxicity.[3]
Flunitrazepam 1991 France Abuse.[3]
Terodiline (Micturin) 1991 Germany, UK, Spain,
others
Prolonged QT interval,
ventricular tachycardia and
arrhythmia.[3]
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Triazolam 1991
France, Netherlands,
Finland, Argentina, UK
others
Psychiatric adverse drug
reactions, amnesia.[3][56]
Benzarone 1992 Germany Hepatitis.[3]
Temafloxacin 1992 Germany, UK, US, others
Low blood sugar; hemolytic
anemia; kidney, liver
dysfunction; allergic
reactions[2][3]
Temafloxacin 1992 US
Allergic reactions and cases
of hemolytic anemia, leading
to three patient deaths.[2]
Bendazac 1993 Spain Hepatotoxicity.[3]
Flosequinan (Manoplax) 1993 UK, US
Increased mortality at higher
doses; increased
hospitalizations.[2][3]
Ketorolac 1993 France, Germany, others Hemorrhage, renal Failure.[3]
Moxisylyte 1993 France Necrotic hepatitis.[3]
Remoxipride 1993 UK, others Aplastic anemia.[3]
Sorivudine 1993 Japan Drug interaction and
deaths.[50]
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Thiobutabarbitone 1993 Germany Renal insufficiency.[3]
Alpidem (Ananxyl) 1995 Worldwide
Not approved in the US,
withdrawn in France in
1994[4]and the rest of the
market in 1995 because of
rare but
serious hepatotoxicity.[3][5]
Chlormezanone (Trancopal) 1996 European Union, US,
South Africa, Japan
Hepatotoxicity; Steven-
Johnson Syndrome; Toxic
Epidermal Necrolysis.[3]
Minaprine 1996 France Convulsions.[3]
Tolrestat (Alredase) 1996 Argentina, Canada, Italy,
others Severe hepatotoxicity[3]
Dexfenfluramine 1997 European Union, UK, US Cardiac valvular disease.[3]
Fen-phen (popular combination
of fenfluramine and phentermin
e)
1997 Cardiotoxicity
Fenfluramine 1997
European Union, UK, US,
India, South Africa,
others
Cardiac valvular disease,
pulmonary hypertension,
cardiac fibrosis.[3][21]
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Pemoline (Cylert) 1997 Canada, UK
Withdrawn from US in 2005.
Hepatotoxicity[31]Reason:hep
atotoxicity.[3]
Phenolphthalein 1997 US Carcinogenicity.[33]
Terfenadine (Seldane,
Triludan)
1997
-
1998
France, South Africa,
Oman, others, US
Prolonged QT interval;
ventricular tachycardia[2][3]
Bromfenac 1998 US
Severe hepatitis and liver
failure (some requiring
transplantation).[2]
Ebrotidine 1998 Spain Hepatotoxicity.[3]
Mibefradil 1998 European Union,
Malaysia, US, others
Fatal arrhythmia, drug
interactions.[2][3]
Proxibarbal 1998 Spain, France, Italy,
Portugal, Turkey
Immunoallergic,
thrombocytopenia.[3]
Sertindole 1998 European Union Arrhythmia and sudden
cardiac death[3][38]
Tolcapone (Tasmar) 1998 European Union,
Canada, Australia Hepatotoxicity[3]
Amineptine (Survector) 1999 France, US Hepatotoxicity, dermatologic
al side effects,
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and abusepotential.[6] Reaso
n:
Aminopyrine 1999 France, Thailand risk of agranulocytosis;
severe acne.[3]
Astemizole (Hismanal) 1999 US, Malaysia, Multiple
Nonspecified Markets Fatal arrhythmia[2][3]
Grepafloxacin (Raxar) 1999 Withdrawn Germany, UK,
US others
Cardiac repolarization; QT
interval prolongation.[2]
Levamisole (Ergamisol) 1999 US
Still used as veterinary drug
and as a human
antihelminthic in many
markets; listed on the WHO
List of Essential Medicines.
In humans, it was used to
treat melanoma before it was
withdrawn
for agranulocytosis.[23][24][25]
Temazepam (Restoril,
Euhypnos, Normison,
Remestan, Tenox, Norkotral)
1999 Sweden, Norway
Diversion, abuse, and a
relatively high rate of
overdose deaths in
comparison to other drugs of
its group. This drug
continues to be available in
most of the world including
the US, but under strict
controls.
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Trovafloxacin (Trovan)
1999
-
2001
European Union, US Withdrawn because of risk
of liver failure[2][3]
Alosetron (Lotronex) 2000 US
Serious gastrointestinal
adverse events; ischemic
colitis; severe
constipation.[2] Reintroduced
2002 on a restricted
basis[citation needed]
Cisapride (Propulsid) 2000 US Risk of fatal cardiac
arrhythmias[2]
Phenylpropanolamine(Propage
st,Dexatrim) 2000 Canada, US Hemorrhagic stroke.[34][35]
Troglitazone (Rezulin) 2000 US, Germany Hepatotoxicity[2]
Ardeparin (Normiflo) 2001 US Not for reasons of safety or
efficacy.[7]
Cerivastatin (Baycol, Lipobay) 2001 US Risk of rhabdomyolysis[2]
Rapacuronium (Raplon) 2001 US, multiple markets
Withdrawn in many countries
because of risk of
fatalbronchospasm[2]
Sparfloxacin 2001 US QT prolongation and
phototoxicity.[2]
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Kava Kava 2002 Germany Hepatotoxicity.[12]
Levomethadyl acetate 2003 US Cardiac arrhythmias and
cardiac arrest.[2]
Bezitramide 2004 Netherlands Fatal overdose.[8]
Co-proxamol (Distalgesic) 2004 UK Overdose dangers.
Dofetilide 2004 Germany Drug interactions, prolonged
QT.[12]
Rofecoxib (Vioxx) 2004 Worldwide
withdrawn by MAH. Risk
of myocardial infarction and
stroke[2]
Valdecoxib (Bextra) 2004 US Risk of heart attack and
stroke.[2]
Adderall XR 2005 Canada
Risk of stroke[1] The ban was
later lifted because the death
rate among those taking
Adderall XR was determined
to be no greater than those
not taking Adderall.
Hydromorphone (Palladone,
extended release version) 2005
High risk of accidental
overdose when extended
release version (Palladone)
administered with alcohol.
Standard hydromorphone is
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sold in most of the world
including the US
Natalizumab (Tysabri)
2005
–
2006
US
Voluntarily withdrawn from
US market because of risk
ofProgressive multifocal
leukoencephalopathy (PML).
Returned to market July,
2006.
Thioridazine (Melleril) 2005 Germany, UK
Withdrawn worldwide due to
severe cardiac
arrhythmias[54][55]
Alatrofloxacin 2006 Worldwide
Liver toxicity; serious liver
injury leading to liver
transplant; death.[2]
Gatifloxacin 2006 US Increased risk of
dysglycemia.[2]
Ximelagatran (Exanta) 2006 Germany Hepatotoxicity[12]
Clobutinol 2007 Germany Ventricular arrhythmia, QT-
prolongation.[12]
Lumiracoxib (Prexige)
2007
–
2008
Worldwide Liver damage
Nefazodone 2007 US, Canada, others Branded version withdrawn
by originator in several
SINthetic Pharmaceutical = ‘Poison of the Witch’
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countries in 2007 for
hepatotoxicity. Generic
versions available.[28]
Pergolide (Permax) 2007 US Risk for heart valve
damage.[2]
Tegaserod (Zelnorm) 2007 US
Risk for heart attack, stroke,
and unstable angina.[2] Was
available through a restricted
access program until April
2008.
Aprotinin (Trasylol) 2008 US Increased risk of death.[2]
Rimonabant (Acomplia) 2008 Worldwide Risk of severe depression
and suicide[12]
Efalizumab (Raptiva) 2009 Germany
Withdrawn because of
increased risk of progressive
multifocal
leukoencephalopathy[12]
Propoxyphene (Darvocet/Darv
on) 2010 Worldwide
Increased risk of heart
attacks and stroke.[14]
Gemtuzumab
ozogamicin(Mylotarg) 2010 US
No improvement in clinical
benefit; risk for death.[2]
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Ozogamicin 2010 US
No improvement in clinical
benefit; risk for death; veno-
occlusive disease.[2]
Rosiglitazone (Avandia) 2010 Europe
Risk of heart attacks and
death. This drug continues to
be available in the US
Sibutramine (Reductil/Meridia) 2010
Australia,[39] Canada,[40] C
hina,[41] the European
Union (EU),[42] Hong
Kong,[43] India,[44] Mexico,
New Zealand,[45] the
Philippines,[46] Thailand,[47]
the United
Kingdom,[48] and the
United States[49]
Increased risk of heart attack
and stroke.[2]
Sitaxentan 2010 Germany Hepatotoxicity.[12]
Drotrecogin alfa (Xigris) 2011 Worldwide
Lack of efficacy as shown by
PROWESS-SHOCK
study[17][18][19]
Tetrazepam 2013 European Union Serious cutaneous
reactions.[51]
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Unapproved Prescription Cough, Cold, and
Allergy Products SHARE
TWEET LINKEDIN PIN IT EMAIL PRINT
The drug products on this list were obtained from the Drug Registration and Listing System (DRLS)
in December 2010. For more DRLS Information.
Domestic and foreign establishments that manufacture, repack, or re-label drug products in the
United States are required to register and list all of their commercially marketed drug products with
the FDA (21 U.S.C. § 360 and 21 CFR 207). Many drug firms do not update their drug listing
information with FDA as required by law; consequently, the information in DRLS is both over- and
under-inclusive. Therefore, the list below of unapproved prescription cough/cold/allergy drug
products may include drugs that are no longer being marketed and/or may not include prescription
cough/cold/allergy drug products that are currently being marketed if the drug firm has not listed or
updated their information with DRLS. Any unapproved prescription oral cough/cold/allergy drugs that
are not on this list are not entitled to any grace period and are subject to immediate enforcement
action.
** Incomplete information was submitted to FDA's Drug Registration and Listing system
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
A TAN 12X SUSPENSION PYRILAMINE TANNATE 30 MG 65162 0530
PHENYLEPHRINE TANNATE 5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
ACCUHIST DM GUAIFENESIN 50 MG 66346 0111
DEXTROMETHORPHAN 5 MG
PSEUDOEPHEDRINE 30 MG
BROMPHENIRAMINE 2 MG
ACCUHIST DROPS CHERRY
FLAVOR
CHLORPHENIRAMINE MALEATE 0.8 MG 23589 0004
PSEUDOEPHEDRINE
HYDROCHLORIDE
9 MG
AEROHIST CAPLETS EXTENDED
RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 038739 *082
METHSCOPOLAMINE NITRATE 2.5 MG
AEROHIST EXTENDED RELEASE
TABLETS
CHLORPHENIRAMINE 8 MG 66440 0082
METHSCOPOLAMINE NITRATE 2.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
AEROHIST PLUS EXTENDED
RELEASE CAPLETS
CHLORPHENIRAMINE MALEATE 8 MG 066440 2376
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
AH CHEW SUSPENSION CHLORPHENIRAMINE TANNATE 35 MG 59196 0015
PHENYLEPHRINE TANNATE 25 MG
AH CHEW ULTRA CHEWABLE
TABLET
CHLORPHENIRAMINE TANNATE 10 MG 59196 0115
PHENYLEPHRINE TANNATE 2 MG
AH-CHEW ULTRA PHENYLEPHRINE 2 MG/5ML 59196 0118
CHLORPHENIRAMINE 10
MG/5ML
SINthetic Pharmaceutical = ‘Poison of the Witch’
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE 1.5
MG/5ML
ALAHIST LQ LIQUID DIPHENHYDRAMINE
HYDROCHLORIDE
25 MG 50991 0607
PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG
ALBATUSSIN NN ALCOHOL FREE DEXTROMETHORPHAN
HYDROBROMIDE
10 MG 49326 0289
PYRILAMINE MALEATE 8.85 MG
POTASSIUM
GUAIACOLSULFONATE
75 MG
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
ALDEX D TANNATE FOR ORAL
SUSPENSION
PHENYLEPHRINE
HYDROCHLORIDE
5 MG 65224 0550
SINthetic Pharmaceutical = ‘Poison of the Witch’
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
ALDEX DM FOR ORAL
SUSPENSION
PHENYLEPHRINE
HYDROCHLORIDE
5 MG 65224 0555
PYRILAMINE MALEATE 16 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
ALDEX DM FOR ORAL
SUSPENSION
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 65224 0555
ALDEX TABLETS GUAIFENESIN 650 MG 65224 0650
PHENYLEPHRINE 25 MG
ALLERGY DN II CHLORPHENIRAMINE 4 MG 51991 0534
METHSCOPOLAMINE NITRATE 2.5 MG
METHSCOPOLAMINE NITRATE 2.5 MG 10122 0650
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
ALLERX 10 DAY DOSEPACK
TABLETS
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
ALLERX D TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 10122 *702
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
ALLERX DOSE PACK DF 30
TABLETS
CHLORPHENIRAMINE MALEATE 4 MG 10122 0704
METHSCOPOLAMINE NITRATE 2.5 MG
ALLERX DOSE PACK PE 30
TABLETS
METHSCOPOLAMINE NITRATE 2.5 MG 10122 *705
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
ALLERX DOSEPACK TABLETS CHLORPHENIRAMINE MALEATE 8 MG 54868 5198
METHSCOPOLAMINE NITRATE 2.5 MG
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
ALLFEN DM GUAIFENESIN 400 MG 58605 0401
DEXTROMETHORPHAN 20 MG
ALLRES G TANNATE
SUSPENSION
GUAIFENESIN 200 MG 028595 0602
CARBETAPENTANE CITRATE 7.5 MG
AMBIFED GUAIFENESIN 400 MG 58605 0414
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
AMBIFED DM GUAIFENESIN 400 MG 58605 0415
DEXTROMETHORPHAN 20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE 30 MG
AQUATAB C DEXTROMETHORPHAN 60 MG 63824 0063
GUAIFENESIN 1200 MG
PHENYLEPHRINE 75 MG
AQUATAB C 12 HOUR TIME
RELEASE TABLETS
DEXTROMETHORPHAN
HYDROBROMIDE
25 MG 16881 *120
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
AQUATAB DM TABLETS
EXTENDED RELEASE
DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 063824 *002
GUAIFENESIN 1200 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
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NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
B VEX D SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 68308 0926
PHENYLEPHRINE TANNATE 20 MG
B VEX SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 68308 0922
BEN TANN SUSPENSION DIPHENHYDRAMINE TANNATE 25 MG 68308 0122
BETATAN SUSPENSION CARBETAPENTANE TANNATE 30 MG 66992 0125
BROMPHENIRAMINE TANNATE 4 MG
PHENYLEPHRINE TANNATE 7.5 MG
BIODEC DM DROPS DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 59741 0134
PSEUDOEPHEDRINE
HYDROCHLORIDE
25 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
46
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
BIOTUSS GUAIFENESIN 300 MG 58552 0113
DEXTROMETHORPHAN 15 MG
PHENYLEPHRINE 10 MG
BP 8 GUAIFENESIN 175 MG 42192 0507
DEXTROMETHORPHAN 15 MG
PSEUDOEPHEDRINE 30 MG
BPM PE DM SYRUP BROMPHENIRAMINE MALEATE 2 MG 64376 736
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
DEXTROMETHORPHAN
HYDROBROMIDE
10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
47
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
BPM PSEUDOEPHERINE
EXTENDED RELEASE TABLET
BROMPHENIRAMINE MALEATE 6 MG 064376 *544
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
BPM TABLETS BROMPHENIRAMINE MALEATE 6 MG 064376 *543
BROFED ELIXIR PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG 00682 7777
BROMPHENIRAMINE MALEATE 4 MG
BROMAAPHEDRINE D
SUSPENSION
PHENYLEPHRINE TANNATE 20 MG 68032 0157
BROMPHENIRAMINE TANNATE 12 MG
BROMFED CAPSULES BROMPHENIRAMINE MALEATE 12 MG 054868 1211
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
48
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
BROMFED CAPSULES PHENYLEPHRINE 15 MG 67000 0200
BROMPHENIRAMINE 12 MG
BROMHIST DM PEDIATRIC
SYRUP
BROMPHENIRAMINE MALEATE 2 MG 60258 0446
GUAIFENESIN 50 MG
DEXTROMETHORPHAN
HYDROBROMIDE
5 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
BROMPHENIRAMINE MALEATE
DROPS
BROMPHENIRAMINE MALEATE 1 MG 68032 0324
BROMPHENIRAMINE MALEATE
PSEUDOEPHEDRINE HCL DROPS
PSEUDOEPHEDRINE
HYDROCHLORIDE
7.5 MG 68032 0325
DEXBROMPHENIRAMINE
MALEATE
1 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
49
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
BROMPHENIRAMINE
PHENYLEPHRINE TANNATE
SUSPENSION
BROMPHENIRAMINE 6 MG 62559 6331
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
BROMPHENIRAMINE TANNATE
CHEWABLE TABLETS
BROMPHENIRAMINE TANNATE 12 MG 68013 0007
BROMPHENIRAMINE TANNATE
SUSPENSION
BROMPHENIRAMINE TANNATE 12 MG 62559 6291
BROMPHERIRAMINE TANNATE
TABLETS
BROMPHENIRAMINE 12 MG 062559 6293
BROMSPIRO LIQUID DOXYLAMINE SUCCINATE 2.5 MG 23359 0010
BROMTUSS DM LIQUID
FORMULA
BROMPHENIRAMINE MALEATE 2 MG 51991 0443
DEXTROMETHORPHAN 15 MG
PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
50
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
BROMUPHED CAPSULES TIME
RELEASE
BROMPHENIRAMINE MALEATE 12 MG 00603 2505
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
BROMUPHED PD CAPSULES
TIME RELEASE
BROMPHENIRAMINE MALEATE 6 MG 00603 2506
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
BRONKIDS LIQUID PHENYLEPHRINE
HYDROCHLORIDE
1.5 MG 49963 0118
CHLORPHENIRAMINE MALEATE 0.6 MG
DEXTROMETHORPHAN
HYDROBROMIDE
2.75 MG
BRONTUSS SF GUAIFENESIN 350 MG 49963 0813
DEXTROMETHORPHAN 15 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
51
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE 10 MG
BROVEX ADT SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 58605 0274
PHENYLEPHRINE TANNATE 10 MG
BROVEX CT BROMPHENIRAMINE TANNATE 12 MG 66813 0273
BROVEX D SUSPENSION BROMPHENIRAMINE TANNATE 12 MG 66813 0274
PHENYLEPHRINE TANNATE 20 MG
BROVEX PD SUSPENSION BROMPHENIRAMINE TANNATE 6 MG 58605 0277
PSEUDOEPHEDRINE TANNATE 30 MG
BROVEX PEB DM LIQUID PHENYLEPHRINE
HYDROCHLORIDE
10 MG 58605 0153
BROMPHENIRAMINE MALEATE 4 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
52
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
BROVEX PEB LIQUID PHENYLEPHRINE
HYDROCHLORIDE
10 MG 58605 0152
BROMPHENIRAMINE MALEATE 4 MG
BROVEX PSB DM LIQUID BROMPHENIRAMINE MALEATE 4 MG 58605 0151
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
20 MG
BROVEX PSB LIQUID BROMPHENIRAMINE MALEATE 4 MG 58605 0150
PSEUDOEPHEDRINE
HYDROCHLORIDE
20 MG
BROVEX SR CAPSULES BROMPHENIRAMINE MALEATE 9 MG 66813 *271
SINthetic Pharmaceutical = ‘Poison of the Witch’
53
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
90 MG
C PHEN DM DROPS CHLORPHENIRAMINE MALEATE 1 MG 21695 0625
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG
C PHEN DM DROPS CHLORPHENIRAMINE MALEATE 1 MG 64376 0726
PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
C PHEN DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 64376 0727
SINthetic Pharmaceutical = ‘Poison of the Witch’
54
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG
CHLORPHENIRAMINE MALEATE 4 MG
C PHEN DROPS CHLORPHENIRAMINE MALEATE 1 MG 64376 0728
PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG
C PHEN SYRUP PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG 64376 0729
CHLORPHENIRAMINE MALEATE 4 MG
C TAN D PLUS SUSPENSION BROMPHENIRAMINE TANNATE 5 MG 23359 0007
PHENYLEPHRINE TANNATE 5 MG
C TAN D SUSPENSION BROMPHENIRAMINE TANNATE 4 MG 23359 0006
SINthetic Pharmaceutical = ‘Poison of the Witch’
55
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE TANNATE 5 MG
C TANNA 12D SUSPENSION PHENYLEPHRINE TANNATE 5 MG 66993 0553
PYRILAMINE TANNATE 30 MG
CARBETAPENTANE TANNATE 30 MG
CARBA XP SYRUP CARBETAPENTANE CITRATE 20 MG 58809 0303
GUAIFENESIN 100 MG
CARBATAB 12 TABLETS CARBETAPENTANE CITRATE 60 MG 58809 *615
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
15 MG
CARBETAPENTANE CITRATE 20 MG 58809 0707
SINthetic Pharmaceutical = ‘Poison of the Witch’
56
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CARBATUSS CL LIQUID
RASPBERRY MINT FLAVOR
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
POTASSIUM
GUAIACOLSULFONATE
100 MG
CARBATUSS SYRUP CARBETAPENTANE CITRATE 20 MG 58809 0536
GUAIFENESIN 100 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CARBODEX DM DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG 55654 0028
DEXTROMETHORPHAN
HYDROBROMIDE
4 MG
CARBODEX DM DROPS
PEDIATRIC
DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 55654 0015
SINthetic Pharmaceutical = ‘Poison of the Witch’
57
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
25 MG
CARBODEX DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 55654 0016
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
CARBOFED DM DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
25 MG 50383 0750
DEXTROMETHORPHAN
HYDROBROMIDE
4 MG
CARBOFED DM ORAL DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG 50383 0576
DEXTROMETHORPHAN
HYDROBROMIDE
4 MG
CARBOFED DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 50383 0751
SINthetic Pharmaceutical = ‘Poison of the Witch’
58
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
CARDEC DM DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
25 MG 00603 1060
DEXTROMETHORPHAN
HYDROBROMIDE
4 MG
CARDEC DM DROPS DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 00603 1064
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG
CARDEC DM ORAL DROPS DEXTROMETHORPHAN
HYDROBROMIDE
3 MG 00603 1068
PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG
CHLORPHENIRAMINE MALEATE 1 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
59
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CARDEC DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 00603 1061
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
CARDEC DM SYRUP PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG 00603 1069
CHLORPHENIRAMINE MALEATE 4 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
CARDEC ORAL DROPS PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG 00603 1066
CHLORPHENIRAMINE MALEATE 1 MG
CARDEC SYRUP BROMPHENIRAMINE MALEATE 4 MG 00603 1063
SINthetic Pharmaceutical = ‘Poison of the Witch’
60
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
CARDEC SYRUP PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG 00603 1067
CHLORPHENIRAMINE MALEATE 4 MG
CENTERGY DM PEDIATRIC
DROPS
CHLORPHENIRAMINE MALEATE 1 MG 23359 0015
PHENYLEPHRINE
HYDROCHLORIDE
2 MG
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
CENTERGY PEDIATRIC DROPS PHENYLEPHRINE
HYDROCHLORIDE
2 MG 23359 0014
CHLORPHENIRAMINE MALEATE 1 MG
CERON DM SYRUP CHLORPHENIRAMINE MALEATE 4 MG 60258 0415
SINthetic Pharmaceutical = ‘Poison of the Witch’
61
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
CERON SYRUP PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG 60258 0414
CHLORPHENIRAMINE MALEATE 4 MG
CERTUSS D SUSTAINED RELEASE
TABLETS
DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 64543 *175
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
CERTUSS MULTILAYER
EXTENDED RELEASE TABLET
CARBETAPENTANE CITRATE 60 MG 64543 *180
GUAIFENESIN 1200 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
62
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CHLOR MES D LIQUID METHSCOPOLAMINE NITRATE 0.625 MG 60258 0221
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CHLORPHENIRAMINE MALEATE 2 MG
CHLOR PSEUDO CAPSULES
EXTENDED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 00440 8255
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
CHLORDEX GP SYRUP CHLORPHENIRAMINE MALEATE 2 MG 60258 0246
GUAIFENESIN 100 MG
DEXTROMETHORPHAN
HYDROBROMIDE
7.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
63
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CHLORFED A SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 55289 *284
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
CHLORPHENIRAMINE MALEATE
AND PSEUDOEPHEDRINE
HYDROCHLORIDE CAPSULES
EXTENDED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 00185 1304
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
CHLORPHENIRAMINE MALEATE
CAPSULES EXTENDED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 00603 2784
CHLORPHENIRAMINE MALEATE
CAPSULES EXTENDED RELEASE
CHLORPHENIRAMINE MALEATE 12 MG 00603 2785
CHLORPHENIRAMINE
PHENYLEPHRINE DM SYRUP
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG 54569 5803
CHLORPHENIRAMINE MALEATE 4 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
64
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
COLDAMINE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 10149 *229
METHSCOPOLAMINE NITRATE 2.5 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
90 MG
COLDMIST DM TABLETS
EXTENDED RELEASE
DEXTROMETHORPHAN
HYDROBROMIDE
32 MG 51991 *146
GUAIFENESIN 595 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
48 MG
COLDMIST LA EXTENDED
RELEASE TABLETS
GUAIFENESIN 795 MG 51991 *367
PSEUDOEPHEDRINE
HYDROCHLORIDE
85 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
65
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
COLFED A CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 51991 *145
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
CORFEN DM LIQUID PHENYLEPHRINE
HYDROCHLORIDE
10 MG 60258 0238
CHLORPHENIRAMINE MALEATE 4 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
CORYZA D TABLETS DEXCHLORPHENIRAMINE
MALEATE
3.5 MG 68047 *271
PSEUDOEPHEDRINE 45 MG
METHSCOPOLAMINE NITRATE 1 MG
CORYZA DM SYRUP PHENYLEPHRINE
HYDROCHLORIDE
5 MG 68047 0270
SINthetic Pharmaceutical = ‘Poison of the Witch’
66
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXCHLORPHENIRAMINE
MALEATE
1.25 MG
DEXTROMETHORPHAN
HYDROBROMIDE
5 MG
PYRILAMINE MALEATE 5 MG
CORZALL LIQUID PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG 63717 0552
CARBETAPENTANE CITRATE 20 MG
CP DEC DM ORAL DROPS CHLORPHENIRAMINE MALEATE 1 MG 50383 0873
PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
CP DEC DM SYRUP CHLORPHENIRAMINE MALEATE 4 MG 50383 0872
SINthetic Pharmaceutical = ‘Poison of the Witch’
67
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
CP DEC ORAL DROPS CHLORPHENIRAMINE MALEATE 1 MG 50383 0871
PHENYLEPHRINE
HYDROCHLORIDE
3.5 MG
C-PHEN DM DEXTROMETHORPHAN
HYDROBROMIDE
3 MG 23490 7848
PHENYLEPHRINE 3 MG
CHORPHENIRAMINE MALEATE 1 MG
CPM PSE SYRUP PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG 64376 0714
CHLORPHENIRAMINE MALEATE 2 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
68
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CYPROHEPTADINE HCL CYPROHEPTADINE HCL 4 MG 00440 7360
D TAB SUSTAINED RELEASE
TABLETS
GUAIFENESIN 1200 MG 24518 *001
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
DA CHEWABLE TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 64455 0013
CHLORPHENIRAMINE MALEATE 2 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
DALLERGY CAPLETS CHLORPHENIRAMINE 12 MG 00277 0182
PHENYLEPHRINE 20 MG
METHSCOPOLAMINE NITRATE 2.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
69
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DALLERGY DROPS PHENYLEPHRINE
HYDROCHLORIDE
2 MG 16477 0120
CHLORPHENIRAMINE MALEATE 1 MG
DALLERGY JR CAPSULES PHENYLEPHRINE 20 MG 00277 0183
CHLORPHENIRAMINE 4 MG
DALLERGY PE SYRUP CHLORPHENIRAMINE MALEATE 2 MG 16477 0821
METHSCOPOLAMINE NITRATE 0.75 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
DALLERGY PSE ER TABLETS PSEUDOEPHEDRINE 60 MG 16477 0146
CLORPHENIRAMINE 4 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
70
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE NITRATE 1.25 MG
DALLERGY SYRUP METHSCOPOLAMINE NITRATE 0.75 MG 16477 0819
PHENYLEPHRINE
HYDROCHLORIDE
8 MG
CHLORPHENIRAMINE MALEATE 2 MG
DALLERGY TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 00277 0160
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CHLORPHENIRAMINE MALEATE 4 MG
DE CHLOR DM LIQUID PHENYLEPHRINE
HYDROCHLORIDE
10 MG 60258 0239
CHLORPHENIRAMINE MALEATE 2 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
71
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
DE CHLOR DR LIQUID CHLORPHENIRAMINE MALEATE 2 MG 60258 0240
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PHENYLEPHRINE
HYDROCHLORIDE
6 MG
DE CONGESTINE SUSTAINED
RELEASE CAPSULES
CHLORPHENIRAMINE 8 MG 00603 3143
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
DECON E LIQUID GUAIFENESIN 100 MG 51724 0014
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
DECON G DROPS GUAIFENESIN 40 MG 51724 0214
SINthetic Pharmaceutical = ‘Poison of the Witch’
72
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
2 MG
BROMPHENIRAMINE MALEATE 1 MG
DECONAMINE SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 54868 1014
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
DECONAMINE SR CAPSULES
SUSTAINED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 00482 0181
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
DECONAMINE SYRUP PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG 00482 0185
CHLORPHENIRAMINE MALEATE 2 MG
DECONAMINE TABLETS PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG 00482 0184
SINthetic Pharmaceutical = ‘Poison of the Witch’
73
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CHLORPHENIRAMINE MALEATE 4 MG
DECONEX TABLETS GUAIFENESIN 900 MG 50991 *306
PHENYLEPHRINE
HYDROCHLORIDE
30 MG
DECONGEST II TABLETS GUAIFENESIN 600 MG 00603 3116
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
DECONOMED SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 61646 *300
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
DEFEN LA TABLETS GUAIFENESIN 600 MG 59630 *110
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
74
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEX PC SYRUP PHENYLEPHRINE
HYDROCHLORIDE
6 MG 64376 0711
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
CHLORPHENIRAMINE MALEATE 2 MG
DEXCHLORPHENIRAMINE
MALEATE TABLETS
DEXCHLORPHENIRAMINE
MALEATE
4 MG 00591 4008
DEXCHLORPHENIRAMINE
MALEATE TABLETS
DEXCHLORPHENIRAMINE
MALEATE
4 MG 00603 3198
DEXCHLORPHENIRAMINE
MALEATE TABLETS
DEXCHLORPHENIRAMINE
MALEATE
6 MG 00603 3199
DEXODRYL CHEWABLE TABLET CHLORPHENIRAMINE TANNATE 2 MG 59196 0117
DEXODRYL SUSPENSION CHLORPHENIRAMINE TANNATE 2 MG 59196 0116
DEXPHEN M ORAL SOLUTION METHSCOPOLAMINE NITRATE 1.25 MG 64376 0737
SINthetic Pharmaceutical = ‘Poison of the Witch’
75
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXCHLORPHENIRAMINE
MALEATE
1 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
DEXTRO PHENYL PYRIL LIQUID PHENYLEPHRINE 15.5 MG 68032 0327
PYRILAMINE 15.5 MG
DEXTROMETHORPHAN HBR
CHLORPHENIRAMINE MALEATE
PHENYLEPHRINE HCL LIQUID
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 68032 0168
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CHLORPHENIRAMINE MALEATE 4 MG
DEXTROMETHORPHAN
TANNATE PHENYLEPHRINE
TANNATE
DEXTROMETHORPHAN 30 MG 68032 0307
PHENYLEPHRINE 20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
76
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXCHLORPHENIRAMINE
TANNATE DEXCHLORPHENIRAMINE 2 MG
DHISTINE SYRUP PHENYLEPHRINE
HYDROCHLORIDE
10 MG 60258 0220
CHLORPHENIRAMINE MALEATE 2 MG
METHSCOPOLAMINE NITRATE 1.25 MG
DIPHENMAX TABLETS
CHEWABLE
DIPHENHYDRAMINE TANNATE 25 MG 68032 0189
DONATUSSIN DM DROPS PHENYLEPHRINE
HYDROCHLORIDE
1.5 MG 16477 0811
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
CHLORPHENIRAMINE MALEATE 1 MG
DONATUSSIN DM SUSPENSION DEXTROMETHORPHAN
TANNATE
30 MG 16477 0130
SINthetic Pharmaceutical = ‘Poison of the Witch’
77
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE TANNATE 20 MG
DEXCHLORPHENIRAMINE
TANNATE
2 MG
DONATUSSIN DROPS GUAIFENESIN 20 MG 16477 0106
PHENYLEPHRINE
HYDROCHLORIDE
1.5 MG
DONTATUSSIN DM SYRUP GUAIFENESIN 150 MG 16477 0132
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
DOXYTEX SYRUP DOXYLAMINE SUCCINATE 2.5 MG 23359 0011
DRIHIST SR TABLETS CHLORPHENIRAMINE MALEATE 8 MG 066993 *110
SINthetic Pharmaceutical = ‘Poison of the Witch’
78
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
DRITUSS DM ELIXIR GUAIFENESIN 200 MG 00603 1181
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
DRITUSS GF TABLETS GUAIFENESIN 1200 MG 00603 3504
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
DRYSEC TABLETS CHLORPHENIRAMINE MALEATE 8 MG 12539 *727
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
79
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DURA VENT DA TABLETS CHLORPHENIRAMINE MALEATE 8 MG 64455 *008
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
DURADRYL CHEWABLE TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 51991 0591
CHLORPHENIRAMINE MALEATE 2 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
DURAVENT DA TABLETS
EXTENDED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 33753 *101
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
METHSCOPOLAMINE NITRATE 2.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
80
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DURAVENT DPB SYRUP PHENYLEPHRINE
HYDROCHLORIDE
5 MG 33753 0105
BROMPHENIRAMINE MALEATE 2 MG
DEXTROMETHORPHAN
HYDROBROMIDE
10 MG
DYNAHIST ER CAPSULES
PEDIATRIC
CHLORPHENIRAMINE MALEATE 4 MG 51991 *217
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
DYNATUSS-EX GUAIFENESIN 200 MG 51991 0211
DEXTROMETHORPHAN 30 MG
PHENYLEPHRIN 10 MG
DYNEX 12 SUSPENSION CARBETAPENTANE TANNATE 22.5 MG 66813 0038
SINthetic Pharmaceutical = ‘Poison of the Witch’
81
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE TANNATE 9 MG
DYNEX TABLETS GUAIFENESIN 1200 MG 66813 *033
PSEUDOEPHEDRINE
HYDROCHLORIDE
90 MG
ED A HIST DM LIQUID BANANA
FLAVOR
CHLORPHENIRAMINE MALEATE 4 MG 00485 0071
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
ED A HIST LIQUID CHLORPHENIRAMINE MALEATE 4 MG 00485 0055
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
ED A-HIST TABLETS CHLORPHENIRAMINE MALEATE 8 MG 00485 0054
SINthetic Pharmaceutical = ‘Poison of the Witch’
82
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
ED CHLOR TAN CAPLETS CHLORPHENIRAMINE TANNATE 8 MG 00485 0072
ED CHLORPED FOR SUSPENSION CHLORPHENIRAMINE TANNATE 2 MG 00485 0074
ENDACON DM EXTENDED
RELEASE TABLET
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 28595 *100
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
ENDAL HD SYRUP CHERRY
FLAVOR
PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG 23589 *008
DIPHENHYDRAMINE
HYDROCHLORIDE
12.5 MG
GUAIFENESIN 800 MG 66813 *535
SINthetic Pharmaceutical = ‘Poison of the Witch’
83
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
ENTEX LA EXTENDED RELEASE
TABLET
PHENYLEPHRINE
HYDROCHLORIDE
30 MG
ENTEX PSE EXTENDED RELEASE
TABLET
GUAIFENESIN 525 MG 66813 *525
PSEUDOEPHEDRINE
HYDROCHLORIDE
50 MG
ENTEX SUSPENSION PSEUDOEPHEDRINE TANNATE 22.5 MG 66813 0555
EXALL D LIQUID GUAIFENESIN 100 MG 63717 0555
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
CARBETAPENTANE CITRATE 10 MG
EXALL PLUS LIQUID GUAIFENESIN 100 MG 63717 0554
CARBETAPENTANE CITRATE 10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
84
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
EXECOF TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 68047 *170
GUAIFENESIN 1000 MG
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
EXEFEN DM SUSTAINED
RELEASE TABLETS
DEXTROMETHORPHAN
HYDROBROMIDE
55 MG 68047 *151
GUAIFENESIN 1000 MG
EXEFEN EXTENDED RELEASE
TABLET
DEXTROMETHORPHAN
HYDROBROMIDE
40 MG 68047 *153
GUAIFENESIN 780 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
80 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
85
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
EXEFEN IR TABLETS PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG 68047 0154
GUAIFENESIN 400 MG
EXEFEN PD EXTENDED RELEASE
TABLETS
GUAIFENESIN 600 MG 68047 *150
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
EXETUSS DM EXTENDED
RELEASE TABLET
DEXTROMETHORPHAN
HYDROBROMIDE
25 MG 68047 *183
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
EXPECTUSS LIQUID CARBETAPENTANE CITRATE 20 MG 23359 0003
GUAIFENESIN 75 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
86
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
EXTENDRYL CHEWABLE
TABLETS
METHSCOPOLAMINE NITRATE 1.25 MG 14629 0103
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CHLORPHENIRAMINE MALEATE 2 MG
EXTENDRYL GCP ORAL
SOLUTION
GUAIFENESIN 100 MG 14629 0105
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
CARBETAPENTANE CITRATE 15 MG
EXTENDRYL JR CAPSULES CHLORPHENIRAMINE MALEATE 4 MG 14629 *102
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
87
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
EXTENDRYL SYRUP DEXCHLORPHENIRAMINE
MALEATE
1 MG 14629 0114
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
EXTENDRYL TABLETS
SUSTAINED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 14629 *101
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
FENESIN DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 64455 *014
GUAIFENESIN 600 MG
GANI TUSS DM NR LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
10 MG 60258 0262
SINthetic Pharmaceutical = ‘Poison of the Witch’
88
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
GUAIFENESIN 100 MG
GANIDIN NR LIQUID GUAIFENESIN 100 MG 60258 0256
G-BID DM TR TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 064376 *542
GUAIFENESIN 1200 MG
GENETUSS 2 SYRUP GUAIFENESIN 300 MG 65615 0426
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
GENTEX 30 LIQUID CARBETAPENTANE CITRATE 30 MG 15014 0888
GUAIFENESIN 200 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
89
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
8 MG
GENTEX LA TABLETS SUSTAINED
RELEASE
GUAIFENESIN 650 MG 15014 *002
PHENYLEPHRINE
HYDROCHLORIDE
23.75 MG
GENTEX LQ SYRUP PHENYLEPHRINE
HYDROCHLORIDE
10 MG 15014 0001
CARBETAPENTANE CITRATE 20 MG
GUAIFENESIN 100 MG
GFN 580 PSEH 60 00 EXTENDED
RELEASE TABLETS
GUAIFENESIN 580 MG 58605 0614
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
GFN AND DM TABLETS GUAIFENESIN 800 MG 60258 0292
SINthetic Pharmaceutical = ‘Poison of the Witch’
90
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN 30 MG
GILTUSS GUAIFENESIN 300 MG 58552 0108
DEXTROMETHORPHAN 15 MG
PHENYLEPHRINE 10 MG
GILTUSS PEDIATRIC GUAIFENESIN 50
MG/1ML
58552 0107
DEXTROMETHORPHAN 5 MG/ML
PHENYLEPHRINE 2.5
MG/ML
GILTUSS TR GUAIFENESIN 288 MG 58552 0312
DEXTROMETHORPHAN 14 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
91
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE 7 MG
G-PHED TIME RELEASE
CAPSULES
GUAIFENESIN 250 MG 59743 0002
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
GUAIDEX TR TABLETS
EXTENDED RELEASE
CHLORPHENIRAMINE MALEATE 8 MG 66177 *817
DEXTROMETHORPHAN
HYDROBROMIDE
60 MG
GUAIFENESIN 1000 MG
METHSCOPOLAMINE NITRATE 1.25 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
GUAIFENESIN 600 MG 00603 3767
SINthetic Pharmaceutical = ‘Poison of the Witch’
92
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
GUAIFEN PSE EXTENDED
RELEASE TABLETS
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
GUAIFEN PSE TABLETS GUAIFENESIN 600 MG 00603 5668
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
GUAIFENESIN AND
PHENYLEPHRINE HCL SYRUP
PHENYLEPHRINE
HYDROCHLORIDE
5 MG 68032 0276
GUAIFENESIN 200 MG
GUAIFENESIN DM NR LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
10 MG 54838 0124
GUAIFENESIN 100 MG
GUAIFENESIN DM NR LIQUID GUAIFENESIN 100 MG 62305 0400
DEXTROMETHORPHAN
HYDROBROMIDE
10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
93
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
GUAIFENESIN DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 66993 *312
GUAIFENESIN 1000 MG
GUAIFENESIN DM TABLETS
SUSTAINED RELEASE
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 51285 *420
GUAIFENESIN 600 MG
GUAIFENESIN LA CAPLETS GUAIFENESIN 600 MG 00904 7759
GUAIFENESIN LA TABLETS GUAIFENESIN 600 MG 64376 *501
GUAIFENESIN LA TABLETS GUAIFENESIN 600 MG 51655 0948
GUAIFENESIN NR LIQUID GUAIFENESIN 100 MG 54838 0123
GUAIFENESIN NR LIQUID GUAIFENESIN 100 MG 62305 0401
SINthetic Pharmaceutical = ‘Poison of the Witch’
94
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
GUAIFENESIN SUSTAINED
RELEASE TABLETS
GUAIFENESIN 1200 MG 00603 3773
GUAIFENESIN SYRUP ALCOHOL
FREE AND SUGAR FREE
GUAIFENESIN 100 MG 60432 0079
GUAIFENESIN TABLETS GUAIFENESIN 200 MG 00904 5154
GUAIFENESIN TABLETS GUAIFENESIN 1000 MG 66993 *320
GUAIFENESIN TABLETS
SUSTAINED RELEASE
GUAIFENESIN 600 MG 51285 *417
GUAIFENESIN TR TABLETS GUAIFENESIN 600 MG 61646 *125
GUAIFENSIN LA TABLETS GUAIFENESIN 600 MG 57664 *152
GUAIPHEN-D TR TABLETS GUAIFENESIN 600 MG 64376 *540
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
95
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
GUAPHEN II DM TABLETS
EXTENDED RELEASE
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG 68032 *134
GUAIFENESIN 800 MG
GUIADEX DM LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 51991 0087
POTASSIUM
GUAIACOLSULFONATE
300 MG
GUIADEX PD EXTENDED
RELEASE TABLETS
GUAIFENESIN 600 MG 51991 *090
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
GUIADRINE DX LIQUID GUAIFENESIN 225 MG 51991 0633
DEXTROMETHORPHAN
HYDROBROMIDE
25 MG
GUIADRINE GP TABLETS GUAIFENESIN 1200 MG 51991 *058
SINthetic Pharmaceutical = ‘Poison of the Witch’
96
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
GUIATEX PE SYRUP GUAIFENESIN 200 MG 51991 0597
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
HEXAFED TABLETS DEXCHLORPHENIRAMINE
MALEATE
4 MG 68220 *027
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
HISTACOL DM PEDIATRIC
SYRUP
GUAIFENESIN 50 MG 51991 0163
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
DEXTROMETHORPHAN
HYDROBROMIDE
5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
97
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
BROMPHENIRAMINE MALEATE 2 MG
HISTEX LIQUID CHLORPHENIRAMINE MALEATE 2 MG 23589 0002
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
HISTEX LIQUID PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG 67336 0275
CHLORPHENIRAMINE MALEATE 2 MG
HISTEX SR CAPSULES BROMPHENIRAMINE MALEATE 10 MG 67336 *089
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
HT TUSS DM ELIXIR GUAIFENESIN 200 MG 50383 0135
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
98
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
HUMIBID DM TABLETS GUAIFENESIN 600 MG 52959 0129
DEXTROMETHORPHAN 30 MG
HYDRO PRO DM SR TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 51991 *243
GUAIFENESIN 600 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
IOBID DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 61646 *112
GUAIFENESIN 600 MG
IOPHEN DM NR LIQUID GUAIFENESIN 100 MG 00254 9232
DEXTROMETHORPHAN
HYDROBROMIDE
10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
99
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
IOPHEN DM NR LIQUID GUAIFENESIN 100 MG 00603 1330
DEXTROMETHORPHAN
HYDROBROMIDE
10 MG
IOPHEN NR LIQUID GUAIFENESIN 100 MG 00603 1328
J MAX SYRUP PHENYLEPHRINE
HYDROCHLORIDE
5 MG 64661 0011
GUAIFENESIN 200 MG
J MAX TABLETS GUAIFENESIN 1200 MG 64661 *010
PHENYLEPHRINE
HYDROCHLORIDE
35 MG
J TAN D PD ORAL DROPS BROMPHENIRAMINE MALEATE 1 MG 64661 0032
PSEUDOEPHEDRINE
HYDROCHLORIDE
7.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
100
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
J TAN D SR TABLETS BROMPHENIRAMINE MALEATE 6 MG 64661 *050
PHENYLEPHRINE
HYDROCHLORIDE
30 MG
J TAN D SUSPENSION PHENYLEPHRINE TANNATE 5 MG 64661 0022
BROMPHENIRAMINE TANNATE 4 MG
J TAN D TABLETS CHEWABLE PHENYLEPHRINE TANNATE ** ** 64661 0021
BROMPHENIRAMINE TANNATE ** **
J TAN PD ORAL DROPS BROMPHENIRAMINE MALEATE 1 MG 64661 0031
J TAN SUSPENSION BROMPHENIRAMINE TANNATE 4 MG 64661 0020
LARTUS GUAIFENESIN ** ** 58173 0037
DEXTROMETHORPHAN ** **
SINthetic Pharmaceutical = ‘Poison of the Witch’
101
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE ** **
LEV PSE AND GG EXTENDED
RELEASE CAPSULES
GUAIFENESIN 400 MG 67537 *035
PSEUDOEPHEDRINE
HYDROCHLORIDE
90 MG
LEVALL 12 ORAL SUSPENSION PHENYLEPHRINE TANNATE 25 MG 14629 0304
CARBETAPENTANE TANNATE 30 MG
LEVALL 12 SUSPENSION CARBETAPENTANE TANNATE 30 MG 66813 0180
PHENYLEPHRINE TANNATE 30 MG
LEVALL 12 SUSPENSION PHENYLEPHRINE TANNATE 30 MG 67537 0180
CARBETAPENTANE TANNATE 30 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
102
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
LEVALL LIQUID PHENYLEPHRINE
HYDROCHLORIDE
15 MG 66813 0179
GUAIFENESIN 100 MG
CARBETAPENTANE CITRATE 20 MG
LIQUIBID PD TABLETS GUAIFENESIN 275 MG 64543 *146
PHENYLEPHRINE
HYDROCHLORIDE
25 MG
LIQUICOUGH DM LIQUID PSEUDOEPHEDRINE
HYDROCHLORIDE
32 MG 51991 0646
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
GUAIFENESIN 175 MG
LODRANE 12 D TABLETS BROMPHENIRAMINE MALEATE 6 MG 00095 0645
SINthetic Pharmaceutical = ‘Poison of the Witch’
103
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
LODRANE 12 HOUR TABLETS
EXTENDED RELEASE
BROMPHENIRAMINE MALEATE 6 MG 00095 0006
LODRANE 24 HOUR EXTENDED
RELEASE CAPSULES
BROMPHENIRAMINE MALEATE 12 MG 00095 1200
LODRANE 24D CAPSULES
EXTENDED RELEASE
BROMPHENIRAMINE MALEATE 12 MG 00095 1290
PSEUDOEPHEDRINE
HYDROCHLORIDE
90 MG
LODRANE D SUSPENSION PSEUDOEPHEDRINE TANNATE 90 MG 00095 9008
LOHIST 12D TABLETS EXTENDED
RELEASE
BROMPHENIRAMINE MALEATE 6 MG 68047 *122
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
104
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
LOHIST DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
10 MG 68047 0129
BROMPHENIRAMINE MALEATE 2 MG
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
LOHIST PD PEDIATRIC DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
12.5 MG 68047 0011
BROMPHENIRAMINE MALEATE 1 MG
LUSONAL LIQUID PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG 66992 0146
LUSONEX TABLETS GUAIFENESIN 800 MG 66992 *140
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
MAXIPHEN GUAIFENESIN 400 MG 58605 0422
SINthetic Pharmaceutical = ‘Poison of the Witch’
105
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE 10 MG
MAXIPHEN ADT TABLETS CHLORPHENIRAMINE TANNATE 2 MG 66870 0030
DEXTROMETHORPHAN
TANNATE
30 MG
PHENYLEPHRINE TANNATE 20 MG
MAXIPHEN DM GUAIFENESIN 400 MG 58605 0423
DEXTROMETHORPHAN 20 MG
PHENYLEPHRINE 10 MG
MAXI-TUSS DM GUAIFENESIN 200 MG 58605 0522
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
106
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
MEDENT DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 45985 *641
GUAIFENESIN 800 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
MEDENT LD TABLETS GUAIFENESIN 800 MG 45985 *642
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
MINTEX PSEUDOEPHEDRINE
HYDROCHLORIDE
30
MG/5ML
51991 0226
CHLORPHENIRAMINE MALEATE 2 MG/5ML
MINTUSS DR LIQUID DEXCHLORPHENIRAMINE
MALEATE
2 MG 51991 0286
SINthetic Pharmaceutical = ‘Poison of the Witch’
107
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PHENYLEPHRINE
HYDROCHLORIDE
6 MG
MONTEPHEN TABLETS GUAIFENESIN 600 MG 12162 *701
PHENYLEPHRINE
HYDROCHLORIDE
25 MG
MUCO FEN DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 59310 *119
GUAIFENESIN 1000 MG
MYHIST DM LIQUID PYRILAMINE MALEATE 12.5 MG 68047 0230
DEXTROMETHORPHAN
HYDRIODIDE
15 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
108
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG
NALDEX TABLETS PHENYLEPHRINE
HYDROCHLORIDE
18.5 MG 51674 0307
DEXCHLORPHENIRAMINE
MALEATE
3.5 MG
NALEX JR CAPSULES GUAIFENESIN 300 MG 051674 0003
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
NASATAB LA TABLETS GUAIFENESIN 500 MG 00095 0225
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
NASOHIST DM PEDIATRIC
DROPS
PHENYLEPHRINE
HYDROCHLORIDE
2 MG 63717 0291
SINthetic Pharmaceutical = ‘Poison of the Witch’
109
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CHLORPHENIRAMINE MALEATE 1 MG
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
NASOHIST PEDIATRIC DROPS PHENYLEPHRINE
HYDROCHLORIDE
2 MG 63717 0290
CHLORPHENIRAMINE MALEATE 1 MG
NEO DM DROPS CHLORPHENIRAMINE MALEATE 0.75 MG 16477 0620
DEXTROMETHORPHAN
HYDROBROMIDE
2.75 MG
PHENYLEPHRINE
HYDROCHLORIDE
1.75 MG
NEUTRAHIST DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
9 MG 60258 0395
CHLORPHENIRAMINE MALEATE 0.8 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
110
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
NO HIST CHEWABLE TABLETS CHLORPHENIRAMINE MALEATE 2 MG 68047 0166
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
NOHIST CAPLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *160
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
NOHIST DMX SUSTAINED
RELEASE TABLETS
CHLORPHENIRAMINE MALEATE 8 MG 68047 *167
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
CHLORPHENIRAMINE MALEATE 8 MG 68047 *161
SINthetic Pharmaceutical = ‘Poison of the Witch’
111
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
NOHIST EXT EXTENDED
RELEASE CAPLET
METHSCOPOLAMINE NITRATE 2.5 MG
NOHIST PLUS JR TABLETS CHLORPHENIRAMINE MALEATE 4 MG 68047 *165
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
NOHIST PLUS TABLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *163
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
NOREL EX TABLETS GUAIFENESIN 800 MG 52747 *440
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
112
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
NOREL LA ANTIHISTAMINE &
DECONGESTANT TABLETS
CARBINOXAMINE MALEATE 8 MG 52747 *435
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
NORTUSS EX LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
40 MG 51724 0220
GUAIFENESIN 400 MG
OMNIHIST II LA TABLETS CHLORPHENIRAMINE MALEATE 8 MG 59196 *032
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
ORATUSS 12 TABLETS GUAIFENESIN 600 MG 067204 *273
CARBETAPENTANE CITRATE 60 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
113
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
15 MG
ORATUSS LIQUID CARBETAPENTANE CITRATE 20 MG 67204 0210
ORGAN I NR TABLETS GUAIFENESIN 200 MG 00603 4886
ORGANIDIN NR LIQUID GUAIFENESIN 100 MG 00037 4214
ORGANIDIN NR TABLETS GUAIFENESIN 200 MG 00037 4312
P CHLOR GG DROPS NASAL
DECONGESTANT
CHLORPHENIRAMINE MALEATE 1 MG 64376 0707
GUAIFENESIN 20 MG
PHENYLEPHRINE
HYDROCHLORIDE
2 MG
PCM ALLERGY TABLETS CHLORPHENIRAMINE MALEATE 12 MG 64376 *036
SINthetic Pharmaceutical = ‘Poison of the Witch’
114
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
PCM CHEWABLE TABLETS METHSCOPOLAMINE NITRATE 1.25 MG 64376 0530
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CHLORPHENIRAMINE MALEATE 2 MG
PDM GG SYRUP GUAIFENESIN 200 MG 64376 0710
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG
PE HIST DM SYRUP PHENYLEPHRINE
HYDROCHLORIDE
5 MG 68047 0320
SINthetic Pharmaceutical = ‘Poison of the Witch’
115
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
CHLORPHENIRAMINE MALEATE 2 MG
PEDIAHIST DM SYRUP BROMPHENIRAMINE MALEATE 2 MG 64376 0723
GUAIFENESIN 50 MG
DEXTROMETHORPHAN
HYDROBROMIDE
5 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
P-EPHEDRINE-GUAIFEN-DM GUAIFENESIN 100 MG 00677 1800
DEXTROMETHOPHAN
HYDROBROMIDE
15 MG
PHENYLEPHRINE
HYDROCHLORIDE
45 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
116
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENA S 12 SUSPENSION PHENYLEPHRINE TANNATE 7.5 MG 58809 0912
PYRILAMINE TANNATE 10 MG
PHENABID CHLORPHENIRAMINE MALEATE 8 MG 58552 *305
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
PHENABID DM DEXTROMETHORPHAN 30 MG 58552 0306
PHENYLEPHRINE 20 MG
CHLORPHENIRAMINE 8 MG
PHENCARB GG SYRUP CARBETAPENTANE CITRATE 20 MG 64376 0537
GUAIFENESIN 100 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
117
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
PHENYDEX LIQUID GUAIFENESIN 200 MG 59936 0005
PYRILAMINE MALEATE 8.35 MG
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
PHENYL T SUSPENSION PHENYLEPHRINE TANNATE 7.5 MG 64376 0437
PHENYLEPHRINE CM TR
TABLETS
CHLORPHENIRAMINE MALEATE 8 MG 64376 *546
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
GUAIFENESIN 900 MG 66993 0326
SINthetic Pharmaceutical = ‘Poison of the Witch’
118
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE AND
GUAIFENESIN TABLETS
PHENYLEPHRINE 25 MG
POLY HIST DM LIQUID PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG 50991 0126
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PYRILAMINE MALEATE 12.5 MG
POLY TUSSIN DM COUGH
SYRUP
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 50991 0320
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
CHLORPHENIRAMINE MALEATE 2 MG
POLY VENT JR CAPLETS GUAIFENESIN 650 MG 50991 *907
SINthetic Pharmaceutical = ‘Poison of the Witch’
119
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
POLYTAN D SUSPENSION DEXBROMPHENIRAMINE
TANNATE
4 MG 50991 0817
PHENYLEPHRINE TANNATE 2.5 MG
POLYTAN DM SUSPENSION DEXBROMPHENIRAMINE
TANNATE
4 MG 50991 0710
PHENYLEPHRINE TANNATE 25 MG
DEXTROMETHORPHAN
TANNATE
30 MG
POLYTAN SUSPENSION DEXBROMPHENIRAMINE
TANNATE
4 MG 50991 0412
POLYVENT CAPLETS GUAIFENESIN 650 MG 50991 0408
PSEUDOEPHEDRINE 90 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
120
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PRE HIST D TABLETS CHLORPHENIRAMINE MALEATE 8 MG 00682 0100
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
PROLEX DM LIQUID POTASSIUM
GUAIACOLSULFONATE
300 MG 51674 0019
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PROLEX PD TABLETS GUAIFENESIN 600 MG 51674 0126
PHENYLEPHRINE 10 MG
PROSET D TABLETS GUAIFENESIN 600 MG 51674 0127
PHENYLEPHRINE 20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
121
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSE BPM LIQUID PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG 64376 0721
BROMPHENIRAMINE MALEATE 4 MG
PSE CPM CHEWABLE TABLETS PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG 64376 0532
CHLORPHENIRAMINE MALEATE 2 MG
PSEUDO CHLOR SR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 57866 0323
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
PSEUDO CMTR TABLETS CHLORPHENIRAMINE MALEATE 8 MG 64376 *032
METHSCOPOLAMINE NITRATE 2.5 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
122
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDO COUGH SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 64376 0733
GUAIFENESIN 175 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
32 MG
PSEUDO DM GG SYRUP PSEUDOEPHEDRINE
HYDROCHLORIDE
40 MG 64376 0712
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
GUAIFENESIN 100 MG
PSEUDO GG TR EXTENDED
RELEASE TABLET
GUAIFENESIN 595 MG 64376 *033
PSEUDOEPHEDRINE
HYDROCHLORIDE
48 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
123
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDO MAX DMX TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
40 MG 64376 *533
GUAIFENESIN 700 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
80 MG
PSEUDO MAX TABLETS GUAIFENESIN 700 MG 64376 *538
PSEUDOEPHEDRINE
HYDROCHLORIDE
80 MG
PSEUDO/BROMPHEN MALEATE
TABLETS
BROMPHENIRAMINE MALEATE 6 MG 54868 5491
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
PSEUDOEPHEDRINE GG SYRUP GUAIFENESIN 200 MG 64376 0716
PSEUDOEPHEDRINE
HYDROCHLORIDE
40 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
124
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE AND
GUAIFENESIN EXTENDED
RELEASE TABLETS
GUAIFENESIN 1200 MG 66993 *332
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
P-TEX BROMPHENIRAMINE TANNATE 10
MG/5ML
50991 0927
PULMARI GP SYRUP GUAIFENESIN 100 MG 60258 0425
CARBETAPENTANE CITRATE 20 MG
PYRLEX CB SUSPENSION PYRILAMINE TANNATE 12 MG 66813 162
CHLORPHENIRAMINE TANNATE 23 MG
PYRLEX PD SUSPENSION PHENYLEPHRINE TANNATE 9 MG 66813 0163
PYRILAMINE TANNATE 12 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
125
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
Q BID DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 00603 5541
GUAIFENESIN 600 MG
Q BID DM TABLETS EXTENDED
RELEASE
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 00603 5542
GUAIFENESIN 600 MG
Q-BID LA TABLETS GUAIFENESIN 600 MG 00603 5543
QIUNTEX LIQUID GUAIFENESIN 100 MG 00603 1635
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
QUARTUSS DM DROPS
ANTITUSSIVE NASAL
DECONGESTANT
ANTIHISTAMINE
PHENYLEPHRINE
HYDROCHLORIDE
1.5 MG 51991 0537
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
126
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
CHLORPHENIRAMINE MALEATE 1 MG
QUARTUSS SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 51991 0513
GUAIFENESIN 100 MG
CHLORPHENIRAMINE MALEATE 2 MG
PENYLEPHRINE
HYDROCHLORIDE
10 MG
RE DRYLEX JR EXTENDED
RELEASE TABLET
CHLORPHENIRAMINE MALEATE 4 MG 68032 *212
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
RE DRYLEX SYRUP DEXCHLORPHENIRAMINE
MALEATE
1 MG 68032 0211
SINthetic Pharmaceutical = ‘Poison of the Witch’
127
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
METHSCOPOLAMINE NITRATE 1.25 MG
RE PHENYLEPHRINE
GUAIFENESIN LIQUID
GUAIFENESIN 20 MG 68032 0368
PHENYLEPHRINE 1.5 MG
RE ALLERGY AM/PM CHLORPHENIRAMINE MALEATE 8 MG 68032 0139
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
METHSCOPOLAMINE NITRATE 2.5 MG
REDUR PCM SUSPENSION PHENYLEPHRINE TANNATE 25 MG 68032 0207
CHLORPHENIRAMINE TANNATE 35 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
128
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
RELCOF CPM TABLETS CHLORPHENIRAMINE MALEATE 8 MG 35573 *004
METHSCOPOLAMINE NITRATE 2.5 MG
RELCOF PE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 35573 *003
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
RELCOF PSE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 35573 *002
METHSCOPOLAMINE NITRATE 2.5 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
REME HIST DM DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 68032 0192
SINthetic Pharmaceutical = ‘Poison of the Witch’
129
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG
PYRILAMINE MALEATE 12.5 MG
REME TUSSIN DM COUGH
SYRUP
CHLORPHENIRAMINE MALEATE 2 MG 68032 0191
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
PHENYLEPHRINE
HYDROCHLORIDE
5 MG
RESCON BIPHASIC SUSTAINED
RELEASE TABLETS
CHLORPHENIRAMINE MALEATE 12 MG 64543 *096
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
CHLORPHENIRAMINE MALEATE 4 MG 64543 *085
SINthetic Pharmaceutical = ‘Poison of the Witch’
130
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
RESCON JR SUSTAINED RELEASE
TABLETS
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
RESCON MX SUSTAINED
RELEASE TABLETS
CHLORPHENIRAMINE MALEATE 8 MG 64543 *090
METHSCOPOLAMINE NITRATE 2.5 MG
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
RESCON MX TABLETS
SUSTAINED RELEASE RESCON-
ED CAPSULES
DEXCHLORPHENIRAMINE
MALEATE
6 MG 64543 *091
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
CHLORPHENIRAMINE MALEATE 8 MG 11808 *089
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
RESPA 1ST TABLETS GUAIFENESIN 600 MG 60575 *087
SINthetic Pharmaceutical = ‘Poison of the Witch’
131
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
58 MG
RESPA BR TABLETS EXTENDED
RELEASE
BROMPHENIRAMINE MALEATE 11 MG 60575 *786
RESPA DM TABLETS EXTENDED
RELEASE
DEXTROMETHORPHAN
HYDROBROMIDE
28 MG 60575 *078
GUAIFENESIN 600 MG
RESPA PE SUSTAINED RELEASE
TABLETS
GUAIFENESIN 600 MG 60575 *787
PHENYLEPHRINE
HYDROCHLORIDE
18 MG
RESPAHIST II EXTENDED
RELEASE TABLET
BROMPHENIRAMINE MALEATE 6 MG 60575 *619
PHENYLEPHRINE
HYDROCHLORIDE
19 MG
RESPAIRE 60 CAPSULE GUAIFENESIN 200 MG 00277 0174
SINthetic Pharmaceutical = ‘Poison of the Witch’
132
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
RESPAIRE CAPSULES PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG 16477 0306
GUAIFENESIN 150 MG
RESPI TANN G SUSPENSION GUAIFENESIN 200 MG 67336 0188
CARBETAPENTANE CITRATE 7.5 MG
RESPIVENT D TABLETS
RESPIVENT DOSE PACK DF
METHSCOPOLAMINE NITRATE 2.5 MG 24486 *702
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
CHLORPHENIRAMINE MALEATE 8 MG 24486 0704
METHSCOPOLAMINE NITRATE 2.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
133
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
RHINABID CAPSULES PHENYLEPHRINE 15 MG 51991 0092
BROMPHENIRAMINE 12 MG
RONDAMINE DM DROPS DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 00904 5573
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG
RONDEC DM ORAL DROPS DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 64455 0050
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG
RONDEC DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 64455 0024
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
134
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
RONDEC SYRUP BROMPHENIRAMINE MALEATE 4 MG 64455 0061
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
RONDEC-DM DEXTROMETHORPHAN 4 MG/ML 64455 0023
PSEUDOEPHEDRINE 25 MG/ML
CARBINOXAMINE 2 MG/ML
RONDEC-DM DEXTROMETHORPHAN 4 MG/ML 64455 0070
PSEUDOEPHEDRINE 15 MG/ML
CARBINOXAMINE 1 MG/ML
RU TUSS DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 15370 0006
SINthetic Pharmaceutical = ‘Poison of the Witch’
135
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
GUAIFENESIN 100 MG
RU TUSS DM SYRUP PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG 59243 0006
GUAIFENESIN 100 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
RU TUSS DM TABLETS DEXTROMETHORPHAN
HYDROBROMIDE
60 MG 59243 *012
GUAIFENESIN 800 MG
RU TUSS JR TABLETS GUAIFENESIN 600 MG 59243 *017
PSEUDOEPHEDRINE
HYDROCHLORIDE
45 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
136
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
RY T 12 SUSPENSION SYRUP PHENYLEPHRINE TANNATE 5 MG 50383 0864
PYRILAMINE TANNATE 30 MG
RYNA 12 SUSPENSION RYNA 12
TABLETS
PHENYLEPHRINE TANNATE 5 MG 00037 0655
PYRILAMINE TANNATE 30 MG
PHENYLEPHRINE TANNATE 8 MG 00037 0673
PYRILAMINE TANNATE 27 MG
RYNA 12 X TABLETS GUAIFENESIN 200 MG 00037 1708
RYNA 12 X TABLETS PHENYLEPHRINE TANNATE 25 MG 00037 1708
PYRILAMINE TANNATE 60 MG
RYNEZE LIQUID GRAPE CHLORPHENIRAMINE MALEATE 4 MG 24839 0346
SINthetic Pharmaceutical = ‘Poison of the Witch’
137
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE NITRATE 1.25 MG
SCOPOHIST PE TABLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *291
METHSCOPOLAMINE NITRATE 1.25 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
SCOPOHIST SYRUP METHSCOPOLAMINE NITRATE 0.75 MG 68047 0292
CHLORPHENIRAMINE MALEATE 2 MG
PHENYLEPHRINE
HYDROCHLORIDE
8 MG
SCOPOHIST TABLETS CHLORPHENIRAMINE MALEATE 8 MG 68047 *290
METHSCOPOLAMINE NITRATE 1.25 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
138
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
SERADEX LA TABLETS BROMPHENIRAMINE MALEATE 6 MG 28595 *110
PHENYLEPHRINE
HYDROCHLORIDE
19 MG
SILDEC DM LIQUID DROPS DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 54838 0211
PSEUDOEPHEDRINE
HYDROCHLORIDE
25 MG
SILDEC DM ORAL DROPS DEXTROMETHORPHAN
HYDROBROMIDE
4 MG 54838 0530
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG
SILDEC DM ORAL DROPS PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG 54838 0537
SINthetic Pharmaceutical = ‘Poison of the Witch’
139
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
4 MG
SILDEC DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 54838 0212
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
SILDEC PE DM SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 54838 0544
CHLORPHENIRAMINE MALEATE 4 MG
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG
SILDEC PE SYRUP CHLORPHENIRAMINE MALEATE 4 MG 54838 0542
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
140
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
SIMUC DM ELIXIR DEXTROMETHORPHAN
HYDROBROMIDE
25 MG 60258 0426
GUAIFENESIN 225 MG
SINA 12X TABLETS PHENYLEPHRINE TANNATE 25 MG 00037 6301
SINUTUSS DM TABLETS PHENYLEPHRINE
HYDROCHLORIDE
15 MG 59196 0045
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG
GUAIFENESIN 600 MG
SINUVENT PE OMNIHIST LA ** ** 59196 0112
SINUVENT PE TABLETS PHENYLEPHRINE
HYDROCHLORIDE
15 MG 59196 0035
GUAIFENESIN 600 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
141
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
SITREX PD LIQUID PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG 67204 0042
GUAIFENESIN 75 MG
SITREX TABLETS GUAIFENESIN 1200 MG 67204 *064
PHENYLEPHRINE
HYDROCHLORIDE
30 MG
SONAHIST DM PEDIATRIC
DROPS
PHENYLEPHRINE
HYDROCHLORIDE
2 MG 68032 0320
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
CHLORPHENIRAMINE MALEATE 1 MG
SONAHIST PEDIATRIC DROPS CHLORPHENIRAMINE MALEATE 1 MG 68032 0326
PHENYLEPHRINE
HYDROCHLORIDE
2 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
142
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
STAMOIST E EXTENDED
RELEASE TABLETS
GUAIFENESIN 500 MG 58407 0375
PSEUDOEPHEDRINE 120 MG
STATUSS DM DEXTROMETHORPHAN 15
MG/5ML
58407 0721
PHENYLEPHRINE 10
MG/5ML
CHLORPHENIRAMINE 2 MG/5ML
SUCLOR CAPSULES CHLORPHENIRAMINE MALEATE 8 MG 62441 *200
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
SUDAHIST EXTENDED RELEASE
TABLET
CHLORPHENIRAMINE MALEATE 12 MG 68047 *330
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
143
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
SUDATEX DM TABLETS PSEUDOEPHEDRINE
HYDROCHLORIDE
40 MG 68047 0242
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
GUAIFENESIN 400 MG
SUDATEX LIQUID PSEUDOEPHEDRINE
HYDROCHLORIDE
40 MG 68047 0124
GUAIFENESIN 200 MG
SUDATRATE TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 68047 *245
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
SYMPAK PDX CHLORPHENIRAMINE 2 MG 59196 0119
PHENYLEPHRINE 10 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
144
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE 1.5 MG
SYMPAK SINUTUSS AND
OMNIHIST II
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 59196 *120
PHENYLEPHRINE
HYDROCHLORIDE
15 MG
GUAIFENESIN 600 MG
TANA R-12 PHENYLEPHRINE 5 MG/5ML 66239 0180
PYRILAMINE TANNATE 30
MG/5ML
TANABID CHEWABLE CAPLETS BROMPHENIRAMINE 2.2 MG 49963 0610
PHENYLEPHRINE 1.58 MG
TANACOF XR ANTIHISTAMINE
FOR SUSPENSION
BROMPHENIRAMINE TANNATE 12 MG 68047 0142
SINthetic Pharmaceutical = ‘Poison of the Witch’
145
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
TANACOF XR ANTIHISTAMINE
FOR SUSPENSION
BROMPHENIRAMINE TANNATE 8 MG 68047 0142
TANAHIST PD PEDIATRIC DROPS
SUSPENSION
CHLORPHENIRAMINE TANNATE 2 MG 68047 0030
TANNATE 12D S CARBETAPENTANE 30 MG/ML 50383 0841
PHENYLEPHRINE 5 MG/ML
PYRILAMINE 30 MG/ML
TENAR DM SYRUP GUAIFENESIN 200 MG 11528 0120
PSEUDOEPHEDRINE
HYDROCHLORIDE
32 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
TENAR PSE LIQUID GUAIFENESIN 200 MG 11528 0115
SINthetic Pharmaceutical = ‘Poison of the Witch’
146
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
40 MG
TIME HIST QD TABLETS CHLORPHENIRAMINE MALEATE 6 MG 66870 *701
METHSCOPOLAMINE NITRATE 2.5 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
TOURO CC CAPLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 58869 *441
GUAIFENESIN 575 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
60 MG
TOURO CC LD CAPLEST DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 58869 *445
GUAIFENESIN 575 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
147
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
25 MG
TOURO DM TABLETS DEXTROMETHORPHAN
HYDRIODIDE
30 MG 58869 *411
GUAIFENESIN 575 MG
TOURO LA LD CAPLETS GUAIFENESIN 525 MG 58869 *635
PSEUDOEPHEDRINE
HYDROCHLORIDE
50 MG
TOURO LA TABLETS GUAIFENESIN 525 MG 58869 *636
PSEUDOEPHEDRINE
HYDROCHLORIDE
120 MG
TRIALL SYRUP PHENYLEPHRINE
HYDROCHLORIDE
8 MG 51991 0524
CHLORPHENIRAMINE MALEATE 2 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
148
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
METHSCOPOLAMINE NITRATE 0.75 MG
TRIKOF D EXTENDED RELEASE
TABLET
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 60575 *457
GUAIFENESIN 600 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
50 MG
TRIPLEX DM LIQUID PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG 51991 0493
PYRILAMINE MALEATE 12.5 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
TRISPEC DMX LIQUID CHERRY GUAIFENESIN 25 MG 58238 0211
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
149
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
TRISPEC DMX PEDIATRIC DROPS
CHERRY
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 58238 0212
GUAIFENESIN 25 MG
TRISPEC PSE LIQUID GRAPE DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 58238 0213
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
GUAIFENESIN 25 MG
TRISPEC PSE PEDIATRIC DROPS
GRAPE
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 58238 0214
GUAIFENESIN 25 MG
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
150
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
TRITAL DM LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 51991 0131
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
CHLORPHENIRAMINE MALEATE 4 MG
TRITUSS ER CAPLETS DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 00642 0661
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
TRITUSS SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
25 MG 00642 0700
GUAIFENESIN 175 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
151
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
12.5 MG
TUSDEC DM LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 60258 0431
PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG
BROMPHENIRAMINE MALEATE 2 MG
TUSNEL GUAIFENESIN 200 MG 54859 0801
DEXTROMETHORPHAN 15 MG
BROMPHENIRAMINE 2 MG
TUSNEL PEDIATRIC COUGH
SYRUP
GUAIFENESIN 50 MG 54859 0544
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
152
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
5 MG
TUSNEL PEDIATRIC DROPS GUAIFENESIN 50 MG 54859 0602
PSEUDOEPHEDRINE
HYDROCHLORIDE
5 MG
TUSNEL SYRUP GUAIFENESIN 200 MG 54859 0502
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
BROMPHENIRAMINE MALEATE 2 MG
TUSNEL-DM GUAIFENESIN 25 MG/ML 54859 0603
DEXTROMETHORPHAN 5 MG/ML
PSEUDOEPHEDRINE 5 MG/ML
SINthetic Pharmaceutical = ‘Poison of the Witch’
153
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
TUSSAFED EX LIQUID DEXTROMETHORPHAN
HYDROBROMIDE
30 MG 53879 0103
GUAIFENESIN 200 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
TUSSAFED EX SYRUP PHENYLEPHRINE
HYDROCHLORIDE
10 MG 00642 0765
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG
GUAIFENESIN 200 MG
TUSSAFED LA CAPLETS GUAIFENESIN 600 MG 00642 0650
DEXTROMETHORPHAN 30 MG
PSEUDOEPHEDRINE 60 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
154
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
TUSSBID CAPSULES GUAIFENESIN 400 MG 51991 0088
PHENYLEPHRINE 15 MG
TUSSI 12 D TABLETS PHENYLEPHRINE TANNATE 10 MG 00037 0692
CARBETAPENTANE TANNATE 60 MG
PYRILAMINE TANNATE 40 MG
TUSSI 12D S SUSPENSION PYRILAMINE TANNATE 30 MG 00037 0693
PHENYLEPHRINE TANNATE 5 MG
CARBETAPENTANE TANNATE 30 MG
TUSSI PRES SYRUP DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 52083 0233
GUAIFENESIN 200 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
155
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
TUSSIDEX LIQUID GRAPE
FLAVOR
PHENYLEPHRINE
HYDROCHLORIDE
10 MG 64320 0729
GUAIFENESIN 200 MG
DEXTROMETHORPHAN
HYDROBROMIDE
30 MG
TUSSO DM CAPLETS DEXTROMETHORPHAN
HYDROBROMIDE
23 MG 00642 0630
GUAIFENESIN 600 MG
PHENYLEPHRINE
HYDROCHLORIDE
9 MG
TUSSO DMR CAPSULES GUAIFENESIN 288 MG 00642 0645
SINthetic Pharmaceutical = ‘Poison of the Witch’
156
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
DEXTROMETHORPHAN
HYDROBROMIDE
7 MG
TUSSO ZMR CAPSULES GUAIFENESIN 200 MG 00642 0647
CARBETAPENTANE CITRATE 8 MG
TUSSO ZR SYRUP CARBETAPENTANE CITRATE 7.5 MG 00642 0649
GUAIFENESIN 150 MG
V TAN DM GRAPE FLAVORED
SUSPENSION
DEXTROMETHORPHAN
TANNATE
25 MG 50383 0856
PYRILAMINE TANNATE 30 MG
PHENYLEPHRINE TANNATE 12.5 MG
V TANN TABLETS CHEWABLE PYRILAMINE TANNATE 30 MG 51991 0267
SINthetic Pharmaceutical = ‘Poison of the Witch’
157
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE TANNATE 25 MG
VANACOF CD PHENYLEPHRINE 5 MG 58809 0817
DEXCHLORPHENIRAMINE
MALEATE
1 MG
VAZOBID TANNATE
SUSPENSION
PHENYLEPHRINE
HYDROCHLORIDE
10 ML 66992 0230
BROMPHENIRAMINE MALEATE 6 ML
VAZOL D LIQUID PHENYLEPHRINE
HYDROCHLORIDE
7.5 MG 66992 0136
BROMPHENIRAMINE MALEATE 4 MG
VIRATAN DM CHEWABLE
TABLETS
PHENYLEPHRINE TANNATE 25 MG 62559 5742
DEXTROMETHORPHAN
TANNATE
25 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
158
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PYRILAMINE TANNATE 30 MG
VIRATAN DM SUSPENSION PYRILAMINE TANNATE 30 MG 62559 5741
PHENYLEPHRINE TANNATE 12.5 MG
DEXTROMETHORPHAN
TANNATE
25 MG
VIRAVAN DM DEXTROMETHORPHAN 25 MG 66346 0142
PHENYLEPHRINE 25 MG
PYRILAMINE 30 MG
VIRAVAN P TANNATE
SUSPENSION CHERRY
BUBBLEGUM FLAVORED
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG 23589 0011
PYRILAMINE MALEATE 15 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
159
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
VIRAVAN PDM GRAPE
FLAVORED TANNATE
SUSPENSION
PSEUDOEPHEDRINE
HYDROCHLORIDE
15 MG 23589 0013
PYRILAMINE MALEATE 15 MG
DEXTROMETHORPHAN
HYDROBROMIDE
15 MG
VIRAVAN T GRAPE FLAVORED
TABLETS
PYRILAMINE TANNATE 30 MG 66346 0032
PHENYLEPHRINE TANNATE 25 MG
VISONEX TABLETS SUSTAINED
RELEASE
GUAIFENESIN 900 MG 68013 *009
PHENYLEPHRINE 30 MG
VISRX DOSE PACK TABLETS METHSCOPOLAMINE NITRATE 2.5 MG 68013 0014
CHLORPHENIRAMINE MALEATE 8 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
160
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
WE ALLERGY CHLORPHENIRAMINE MALEATE 2 MG 59196 0070
METHSCOPOLAMINE NITRATE 0.625 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
WELLBID D 1200 SUSTAINED
RELEASE TABLETS
GUAIFENESIN 1200 MG 66993 *316
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
WELLBID D SUSTAINED RELEASE
TABLETS
GUAIFENESIN 600 MG 66993 *315
PHENYLEPHRINE
HYDROCHLORIDE
40 MG
Z COF 8DM DEXTROMETHORPHAN
HYDROBROMIDE
15 MG 65224 0616
GUAIFENESIN 175 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
161
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PSEUDOEPHEDRINE
HYDROCHLORIDE
30 MG
Z COF LA TABLETS DEXTROMETHORPHAN
HYDROCHLORIDE
30 MG 65224 *105
GUAIFENESIN 650 MG
Z DEX 12D TABLETS DEXTROMETHORPHAN
HYDROCHLORIDE
30 MG 13811 *003
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
CHLORPHENIRAMINE
HYDROCHLORIDE
8 MG
Z DEX PEDIATRIC DROPS PHENYLEPHRINE
HYDROCHLORIDE
2.5 MG 13811 0001
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
162
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
GUAIFENESIN 35 MG
Z DEX SYRUP GUAIFENESIN 100 MG 13811 0002
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
PHENYLEPHRINE
HYDROCHLORIDE
10 MG
ZOTEX 12 SUSPENSION DEXTROMETHORPHAN
TANNATE
2.5 MG 68025 0024
PHENYLEPHRINE TANNATE 15.5 MG
PYRILAMINE TANNATE 15.5 MG
ZOTEX 12D SUSTAINED RELEASE
TABLETS
DEXTROMETHORPHAN
HYDROCHLORIDE
30 MG 68025 *033
CHLORPHENIRAMINE
HYDROCHLORIDE
8 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
163
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
ZOTEX GP CAPLETS GUAIFENESIN 550 MG 68025 0005
PHENYLEPHRINE
HYDROCHLORIDE
8.5 MG
ZOTEX GPX CAPLETS
EXPECTORANT
GUAIFENESIN 550 MG 68025 *020
PHENYLEPHRINE
HYDROCHLORIDE
8.5 MG
ZOTEX LA CAPLETS DEXTROMETHORPHAN
HYDROBROMIDE
25 MG 68025 *002
GUAIFENESIN 500 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
164
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
ZOTEX LAX CAPLETS DEXTROMETHORPHAN
HYDROBROMIDE
25 MG 68025 *018
GUAIFENESIN 550 MG
PHENYLEPHRINE
HYDROCHLORIDE
20 MG
ZOTEX PE SUSTAINED RELEASE
TABLETS
BROMPHENIRAMINE MALEATE 6 MG 68025 *034
PHENYLEPHRINE
HYDROCHLORIDE
30 MG
ZOTEX PEDIATRIC DROPS PHENYLEPHRINE
HYDROCHLORIDE
2.5 MG 68025 0003
DEXTROMETHORPHAN
HYDROBROMIDE
3 MG
GUAIFENESIN 35 MG
SINthetic Pharmaceutical = ‘Poison of the Witch’
165
NAME OF DRUG INGREDIENTS STRENGTH
NDC
LABELER
CODE
NDC
PRODUCT
CODE
ZOTEX SYRUP PHENYLEPHRINE
HYDROCHLORIDE
10 MG 68025 0001
DEXTROMETHORPHAN
HYDROBROMIDE
20 MG
GUAIFENESIN 100 MG
ZYMINE DRX SUSPENSION PSEUDOEPHEDRINE TANNATE 45 MG 67204 0340
TRIPROLIDINE TANNATE 2.5 MG
ZYMINE XR SUSPENSION TRIPROLIDINE TANNATE 2.5 MG 67204 0325
See also
Adverse drug reaction
Adverse events (AEs)
European Medicines Agency
Food and Drug Administration
SINthetic Pharmaceutical = ‘Poison of the Witch’
166
References
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2. ^ to:a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae Qureshi, ZP; Seoane-Vazquez, E; Rodriguez-Monguio, R; Stevenson, KB; Szeinbach, SL (July 2011). "Market withdrawal of new molecular entities approved in the United States from 1980 to 2009.". Pharmacoepidemiology and drug safety 20 (7): 772–7. doi:10.1002/pds.2155. PMID 21574210.
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h di dj dk Fung, M.; Thornton, A.; Mybeck, K.; Wu, J. H.-h.; Hornbuckle, K.; Muniz, E. (1 January 2001). "Evaluation of the Characteristics of Safety Withdrawal of Prescription Drugs from Worldwide Pharmaceutical Markets-1960 to 1999". Therapeutic Innovation & Regulatory Science 35 (1): 293–317. doi:10.1177/009286150103500134.
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23. Nancy Y Zhu; Donald F. LeGatt; A Robert Turner (February 2009). "Agranulocytosis After Consumption of Cocaine Adulterated With Levamisole". Annals of Internal Medicine150 (4): 287–289. doi:10.1059/0003-4819-150-4-200902170-00102. PMID 19153405. Retrieved 2009-10-07.
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26. "Drug Effects - Methaqualone". South African Police Service. Retrieved 24 September 2013.
27. Cosgrove-Mather, Bootie (December 5, 2007). "Anti-Depressant Taken Off Market". CBS NEWS. Retrieved 29 September 2013.
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28. DrugBank. "Oxeladin". Retrieved 24 September 2013.
29. DrugBank. "Oxyphenbutazone". Retrieved 24 September 2013.
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