Cadila Health - Update on FDA Warning - MOS - 31Dec2015

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31 December 2015 Update | Sector: Healthcare Cadila Health Kumar Saurabh ([email protected]); +91 22 3982 5584 Amey Chalke ([email protected]); +91 22 39825423 BSE SENSEX S&P CNX CMP: INR328 TP: INR380 (+16%) Buy 26,118 7,946 Bloomberg CDH IN Equity Shares (m) 1,023.7 M.Cap. (INR b) / (USD b) 335.8/5.1 52-Week Range (INR) 454/285 1, 6, 12 Rel.Per (%) -18/-4/8 Avg Val (INR m) 284 Free float (%) 25.2 Financials & Valuation (INR billion) Y/E MAR 2016E 2017E 2018E Sales 97.6 111.5 133.2 EBITDA 22.4 23.4 32.0 Net Profit 15.5 14.9 21.5 Adj.EPS (INR) 15.1 14.5 21.0 EPS Gr. (%) 29.4 -3.7 44.5 BV/Sh. (INR) 52.6 62.8 79.5 RoE (%) 31.2 25.2 29.5 RoCE (%) 29.7 26.7 33.2 Payout (%) 23.9 29.0 20.2 Valuations P/E (x) 21.7 22.6 15.6 P/BV (x) 6.2 5.2 4.1 EV/EBITDA(x) 15.4 14.6 10.3 Div. Yield (%) 0.9 1.1 1.1 Moraiya facility receives warning letter; earnings to be hit Early resolution is critical, given that Moraiya remains one of the key facilities for CDH with 60% of US sales. Even though corrective plans were in place, warning letter means additional efforts are needed for plant to become USFDA compliant. Apart from Moraiya facility, CDH has also received warning letter for Ahmedabad-based API facility. However, it currently does not supply any product from this plant and has withdrawn all DMF filings. Delay in key product approvals due to warning letters is likely to result in ~23% cut in FY17 EPS and 18% cut in FY18 EPS. Slowdown in product approvals to continue The management stated that warning letter includes two main observations: 1) Product-specific batch failure, 2) SOP-related issue. USFDA had inspected Moraiya facility in September 2014 and noted four key 483 observations. Since then, CDH has not received any approval for Moraiya plant products. Though no new approvals are expected for products from Moraiya facility in FY17, management expects ~15 ANDA approvals over the next 15-18 months (v/s the earlier expectation of ~25-30 ANDA approvals)—primarily from other USFDA approved facilities. Moraiya the largest USFDA-approved facility for Cadila Apart from Nesher and JVs, Cadila has three USFDA-approved formulation facilitiesMoraiya, SEZ and Baddi. Moraiya facility remains the biggest and contributes more than 60% of US sales. Of the total 159 pending ANDAs, 74 are from this facility, reflecting huge dependence on one facility. The Baddi-based facility was approved recently (May-15) by USFDA and production is expected to ramp up going ahead. USFDA also approved the SEZ facility in 2QFY16 and product approvals are expected to start coming through from this facility in coming quarters. Site transfer plan in place; to transfer four key products Management highlighted that it has already site transferred nine products from marketed portfolio and is likely to file for four more products in 1HCY16, including Asacol HD and Prevacid ODT. Given that Asacol HD’s AG version would be launched in July 16, probability of FTF launch of this drug is low in our view. Having said that, transdermal patches that are expected to get approvals over next two years would not be transferred to any other facility. Delay in key US launches to impact earnings We have cut our FY17/18 EPS by 23%/8%, as we believe Moraiya resolution will take another 12 months. Deferral of key launches to 2HCY16 and incremental hit on margins would lead to earnings cut over the next two years. Having said that, site transfers and launches from other facilities in the US and steady growth in Indian- branded business would drive growth in near term. We maintain Buy on CDH but with lower TP of INR380 @ 18x FY18E P/E (v/s INR505 @ 22x 1H FY17E P/E earlier). Investors are advised to refer through important disclosures made at the last page of the Research Report. Motilal Oswal research is available on www.motilaloswal.com/Institutional-Equities, Bloomberg, Thomson Reuters, Factset and S&P Capital. Estimate change TP change Rating change

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Cadila Health

Transcript of Cadila Health - Update on FDA Warning - MOS - 31Dec2015

31 December 2015

Update | Sector: Healthcare

Cadila Health

Kumar Saurabh ([email protected]); +91 22 3982 5584 Amey Chalke ([email protected]); +91 22 39825423

BSE SENSEX S&P CNX CMP: INR328 TP: INR380 (+16%) Buy 26,118 7,946

Bloomberg CDH IN Equity Shares (m) 1,023.7

M.Cap. (INR b) / (USD b) 335.8/5.1 52-Week Range (INR) 454/285 1, 6, 12 Rel.Per (%) -18/-4/8

Avg Val (INR m) 284 Free float (%) 25.2

Financials & Valuation (INR billion) Y/E MAR 2016E 2017E 2018E

Sales 97.6 111.5 133.2 EBITDA 22.4 23.4 32.0 Net Profit 15.5 14.9 21.5

Adj.EPS (INR) 15.1 14.5 21.0 EPS Gr. (%) 29.4 -3.7 44.5 BV/Sh. (INR) 52.6 62.8 79.5

RoE (%) 31.2 25.2 29.5 RoCE (%) 29.7 26.7 33.2 Payout (%) 23.9 29.0 20.2

Valuations P/E (x) 21.7 22.6 15.6 P/BV (x) 6.2 5.2 4.1

EV/EBITDA(x) 15.4 14.6 10.3 Div. Yield (%) 0.9 1.1 1.1

Moraiya facility receives warning letter; earnings to be hit Early resolution is critical, given that Moraiya remains one of the key facilities for CDH

with 60% of US sales. Even though corrective plans were in place, warning letter means additional efforts are

needed for plant to become USFDA compliant. Apart from Moraiya facility, CDH has also received warning letter for Ahmedabad-based

API facility. However, it currently does not supply any product from this plant and has withdrawn all DMF filings.

Delay in key product approvals due to warning letters is likely to result in ~23% cut in FY17 EPS and 18% cut in FY18 EPS.

Slowdown in product approvals to continue The management stated that warning letter includes two main observations: 1) Product-specific batch failure, 2) SOP-related issue. USFDA had inspected Moraiya facility in September 2014 and noted four key 483 observations. Since then, CDH has not received any approval for Moraiya plant products. Though no new approvals are expected for products from Moraiya facility in FY17, management expects ~15 ANDA approvals over the next 15-18 months (v/s the earlier expectation of ~25-30 ANDA approvals)—primarily from other USFDA approved facilities.

Moraiya the largest USFDA-approved facility for Cadila Apart from Nesher and JVs, Cadila has three USFDA-approved formulation facilities— Moraiya, SEZ and Baddi. Moraiya facility remains the biggest and contributes more than 60% of US sales. Of the total 159 pending ANDAs, 74 are from this facility, reflecting huge dependence on one facility. The Baddi-based facility was approved recently (May-15) by USFDA and production is expected to ramp up going ahead. USFDA also approved the SEZ facility in 2QFY16 and product approvals are expected to start coming through from this facility in coming quarters.

Site transfer plan in place; to transfer four key products Management highlighted that it has already site transferred nine products from marketed portfolio and is likely to file for four more products in 1HCY16, including Asacol HD and Prevacid ODT. Given that Asacol HD’s AG version would be launched in July 16, probability of FTF launch of this drug is low in our view. Having said that, transdermal patches that are expected to get approvals over next two years would not be transferred to any other facility.

Delay in key US launches to impact earnings We have cut our FY17/18 EPS by 23%/8%, as we believe Moraiya resolution will take another 12 months. Deferral of key launches to 2HCY16 and incremental hit on margins would lead to earnings cut over the next two years. Having said that, site transfers and launches from other facilities in the US and steady growth in Indian-branded business would drive growth in near term. We maintain Buy on CDH but with lower TP of INR380 @ 18x FY18E P/E (v/s INR505 @ 22x 1H FY17E P/E earlier).

Investors are advised to refer through important disclosures made at the last page of the Research Report. Motilal Oswal research is available on www.motilaloswal.com/Institutional-Equities, Bloomberg, Thomson Reuters, Factset and S&P Capital.

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Key takeaways from the conference call Warning letters: The company’s facilities in Moraiya and Ahmedabad were

inspected in September 2015 and February 2015, respectively. The inspection culminated into several 483 observations for these facilities. However, as the CDH’s response to these 483 observations was found unsatisfactory, the USFDA issued warning letters to both the facilities.

483 observations: Warning letter highlighted two points for Moraiya facility: 1) Repeated product-specific batch failure (Warfarin supplies were discontinued due to this failure) and 2) SOP-related issues. The Ahmedabad plant witnessed GMP violations; the company has withdrawn all DMFs from the facility and is no longer supplying to the US market.

Priorities post the warning letters: 1) Remediation of both facilities and 2) filing for site transfer of key future products.

Asacol HD: CDH is in the process of filing for site transfer of this product. The company has option to launch Asacol HD AG in market in July 2016. However, in such circumstances, it will lose its right to launch generic Asacol HD under exclusivity. The Management highlighted that generic opportunity could be extended beyond the exclusivity period due to lack of filings. As a result, CDH may choose to file for site transfer rather than launching AG in the market.

Site transfer: CDH has currently transferred nine products from Moraiya facility to Ahmedabad-based SEZ facility from the existing product portfolio. The company is also expected to site transfer four more products from future pipeline, including Asacol HD and Prevacid ODT. CDH also clarified that it might not site transfer transdermal patches that were expected to receive approval over the next two years and wait for Moraiya facility to get FDA clearance.

Revenue exposure: The Moraiya facility currently supplies 60% of the total US sales. In terms of pending product approvals, CDH has filed 74 products from Moraiya facility—which includes 40% of total oral solid filings.

Other inspections: Four other key facilities (Dabasa API, Ankleshwar API, Baddi Formulations and SEZ formulations) were also inspected in 2014/2015 and have not received critical observations from USFDA. The SEZ facility has already received EIR from USFDA and is expected to get product approvals very soon.

Filing and launch timelines delayed: The company indicated that ANDAs filing and launches will be delayed until the issue is resolved. However, the company could continue its filing from other facilities.

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Exhibit 1: Past US FDA enforcement action on Indian companies

Company FDA Action Unit Nature of facility

Date of action

Date of resolution

Resolution in (months)

Cadila Warning Letter Ahmedabad API 31-Dec-2015 x NA

Cadila Warning Letter Moraiya Formulations 31-Dec-2015 x NA

Sun pharma Warning Letter Halol Formulations 19-Dec-2015 X NA

Dr. Reddy's Warning Letter Srikakulam, AP API 6-Nov-15 x NA

Dr. Reddy's Warning Letter Miryalaguda, TL API 6-Nov-15 x NA

Dr. Reddy's Warning Letter Visakhapatnam, AP Formulations 6-Nov-15 x NA

IPCA Labs Import Alert Silvassa, Gujrat Formulations 25-Mar-15 x NA

IPCA Labs Import Alert Pithampur, MP Formulations 25-Mar-15 x NA

Sun Pharma Import Alert Karkhadi, Gujarat API 13-Mar-14 x NA

IPCA Labs Import Alert Ratlam, MP API 23-Jan-15 x NA

Ranbaxy Ban Taonsa API 24-Jan-14 x NA

Ranbaxy Import Alert Mohali Formulations 13-Sep-13 x NA Strides Arcolab Warning Letter Bangalore Injectable formulations 11-Sep-13 x NA

Wockhardt Import Alert Waluj, India Formulations 24-May-13 x NA Jubilant Life Sciences Warning Letter Canada Formulations 27-Feb-13 x NA

Dr. Reddy's Import Alert Mexico API 6-Jul-11 27-Jul-12 12.9

Cadila Warning Letter Moraiya Formulations 6-Jun-11 17-Jul-12 13.6

Aurobindo Warning Letter Unit III Formulations 23-May-11 4-Jun-12 12.6

Aurobindo Import Alert Unit VI Formulations 27-Feb-11 28-Mar-13 25.3

Sun Pharma Warning Letter Able Labs 31-Aug-10 19-Sep-11 12.8

Ranbaxy Warning Letter Ohm Labs Formulations 24-Dec-09 x NA

Sun Pharma Product Seizure Michigan, Caraco Formulations 26-Jun-09 28-Aug-12 38.6

Lupin Warning Letter Mandideep Formulations 14-May-09 20-Jan-10 8.4

Cipla Form '483 Bangalore API 20-Apr-09 31-Aug-09 4.4

Ranbaxy AIP Paonta Sahib Formulations 26-Feb-09 x NA Taro Pharma Warning Letter Brampton,

Canada Formulations 5-Feb-09 25-Apr-11 27.0

Ranbaxy Warning Letter Batamandi API 17-Sep-08 x NA

Ranbaxy Import Alert Dewas Formulations 17-Sep-08 x NA

Source: Company, MOSL

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Story in charts

Exhibit 2: Sales trend

Source: Company, MOSL

Exhibit 3: India business to grow at 12% CAGR

Source: Company, MOSL

Exhibit 4: US business to bounce back in FY18E

Source: Company, MOSL

Exhibit 5: Brazil business to recover from regulatory issues

Source: Company, MOSL

Exhibit 6: Margins to be impacted in FY17E

Source: Company, MOSL

Exhibit 7: Earnings to recover in FY18E (post FDA resolution)

Source: Company, MOSL

28 33 39 48 57 71 79 106 126 3 3 3 3 3

4 4

5 5

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

Formulations (INR b) API (INR b)

14 16 19 23 25 27 30 34 38

12.2 12.1

16.9 22.6

6.1 8.6

12.5 12.0 12.0

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

DF Revenues (INR b) YoY Growth (%)

142 212 261

277

357 560

593 652

802

63

50

23

6

29

57

6 10

23

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

US Revenues (USD m) Growth (%)

2 2 2 2 2 2 2 3 3

12

24

10

-4 -1 0 -4

17 17

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

Brazil Revenues (INR b) YoY Growth (%)

8 10 11 11 12 18

22 23 32

21.9 22.2 20.6 17.7 16.6

20.6 22.9

21.0 24.1

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

EBITDA (INR b) EBITDA Margin

5 6 6 6 8 12 15 15 21 2 1 1 0

0

0

FY 10 FY 11 FY 12 FY 13 FY 14 FY 15 FY 16E FY 17E FY 18E

Core EPS (INR/ share) One Off

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Exhibit 8: Rich ANDA pipeline

Source: Company, MOSL

Exhibit 9: R&D expense to remain elevated

Source: Company, MOSL

Exhibit 10: Return ratios to be impacted in FY17E

Source: Company, MOSL

Exhibit 11: Steady asset turnover ratio

Source: Company, MOSL

92 106 131 148

176 227

270

47 52 66 81 100 139

159

FY09 FY10 FY11 FY12 FY13 FY14 YTD

ANDA filed ANDA pending

2 2 3 4 4 6 7 8 10

5 4 6 6

5 6

7 8 8

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

R&D expense (INR b) % of sales

35.8 37.4

27.5 23.7 25.2

30.8 31.2 25.2

29.5

26.7 30.4

22.9 17.9 18.6

24.9 29.7

26.7 33.2

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

RoE (%) RoCE (%)

16 18 25 29 32 37 46 54 61

2.3 2.5

2.1 2.2 2.3 2.3 2.1 2.0 2.2

FY10 FY11 FY12 FY13 FY14 FY15 FY16E FY17E FY18E

Gross Block (INR b) Fixed Asset turnover

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Financials and valuations

Income Statement (INR Million) Y/E March 2011 2012 2013 2014 2015 2016E 2017E 2018E Net Sales 46,306 52,633 63,579 72,241 86,514 97,596 111,496 133,153 Change (%) 25.6 13.7 20.8 13.6 19.8 12.8 14.2 19.4 Total Expenditure 36,044 41,795 52,327 60,239 68,672 75,232 88,082 101,130

% of Sales 77.8 79.4 82.3 83.4 79.4 77.1 79.0 76.0 EBITDA 10,262 10,838 11,252 12,001 17,841 22,364 23,414 32,023 Margin (%) 22.2 20.6 17.7 16.6 20.6 22.9 21.0 24.1 Depreciation 1,269 1,579 1,847 2,012 2,873 2,962 3,324 3,590 EBIT 8,993 9,259 9,405 9,989 14,969 19,401 20,090 28,433 Int. and Finance Charges 699 1,211 1,262 1,181 613 452 412 367 Other Income - Rec. 131 -107 -55 786 554 1,719 1,267 1,985 PBT before EO Expense 8,425 7,941 8,088 9,594 14,910 20,668 20,945 30,052 EO Expense/(Income) 0 0 0 172 83 -429 0 0 PBT after EO Expense 8,425 7,941 8,088 9,423 14,827 21,097 20,945 30,052 Current Tax 1,064 1,130 1,188 1,060 2,594 5,676 5,655 8,114 Deferred Tax 0 0 0 0 0 0 0 0 Tax 1,064 1,130 1,188 1,060 2,594 5,676 5,655 8,114 Tax Rate (%) 12.6 14.2 14.7 11.2 17.5 26.9 27.0 27.0 Reported PAT 7,361 6,811 6,900 8,363 12,233 15,421 15,290 21,938 Less: Minority Interest 251 286 364 326 377 395 415 436 Net Profit 7,110 6,525 6,536 8,037 11,856 15,025 14,875 21,502 PAT Adj for EO Items 6,333 5,660 6,536 8,208 11,939 15,454 14,875 21,502 Change (%) 24.6 -10.6 15.5 25.6 45.5 29.4 -3.7 44.5 Margin (%) 13.7 10.8 10.3 11.4 13.8 15.8 13.3 16.1

Balance Sheet (INR Million) Y/E March 2011 2012 2013 2014 2015 2016E 2017E 2018E Equity Share Capital 1,024 1,024 1,024 1,024 1,024 1,024 1,024 1,024 Total Reserves 20,691 24,712 28,421 33,366 41,492 52,827 63,274 80,348 Net Worth 21,715 25,736 29,445 34,390 42,516 53,851 64,298 81,372 Minority Interest 669 904 1193 1443 1689 2084 2500 2935 Deferred liabilities 1127 1185 1005 961 586 586 586 586 Total Loans 11,034 21,307 27,946 23,955 23,760 22,260 19,760 17,760 Capital Employed 34,545 49,132 59,589 60,748 68,551 78,782 87,144 102,654

Gross Block 24,004 35,612 38,726 41,380 46,259 55,749 63,493 70,366 Less: Accum. Deprn. 5,331 6,786 8,470 10,142 12,737 15,497 18,783 22,373 Net Fixed Assets 18,673 28,826 30,256 31,238 33,522 40,251 44,711 47,993 Capital WIP 3,963 4,492 7,356 8,915 7,979 4,490 2,745 1,872 Investments 207 242 1,145 866 1,544 1,544 1,544 1,544

Curr. Assets 23,263 30,232 34,965 38,845 47,426 58,543 64,179 80,034 Inventory 8,119 10,905 12,136 13,675 15,357 17,951 20,801 23,571 Account Receivables 7,652 8,863 9,551 11,337 15,884 17,860 20,404 24,367 Cash and Bank Balance 2,952 4,666 5,838 5,488 6,699 13,006 12,982 21,813 Loans & Advances 4,540 5,798 7,440 8,345 9,486 9,727 9,992 10,283 Curr. Liability & Prov. 11,561 14,660 14,133 19,116 21,920 26,046 26,035 28,790 Account Payables 9,379 12,379 11,660 16,189 17,191 19,540 18,680 20,808 Provisions 2,182 2,281 2,473 2,927 4,729 6,506 7,354 7,983 Net Current Assets 11,702 15,572 20,832 19,730 25,506 32,497 38,144 51,244 Appl. of Funds 34,545 49,132 59,589 60,749 68,551 78,781 87,143 102,653 E: MOSL Estimates

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Financials and valuations

Ratios Y/E March 2011 2012 2013 2014 2015 2016E 2017E 2018E Basic (INR)

EPS 6.2 5.5 6.4 8.0 11.7 15.1 14.5 21.0 Cash EPS 8.2 7.9 8.2 9.8 14.4 17.6 17.8 24.5 BV/Share 21.2 25.1 28.8 33.6 41.5 52.6 62.8 79.5 DPS 1.3 1.5 1.5 1.8 2.4 3.0 3.6 3.6 Payout (%) 20.8 27.1 30.5 27.1 24.1 23.9 29.0 20.2

Valuation (x)

P/E 52.5 58.8 40.5 27.9 21.5 22.4 15.5 Cash P/E 39.7 41.1 33.1 22.6 18.5 18.3 13.3 P/BV 15.3 12.9 9.7 7.8 6.2 5.2 4.1 EV/Sales 7.4 6.6 4.8 4.0 3.5 3.0 2.5 EV/EBITDA 33.2 32.2 29.2 19.5 15.2 14.4 10.2 Dividend Yield (%) 0.4 0.5 0.6 0.7 0.9 1.1 1.1

Return Ratios (%)

RoE 37.4 27.5 23.7 25.2 30.8 31.2 25.2 29.5 RoCE 30.4 22.9 17.9 18.6 24.9 29.7 26.7 33.2

Working Capital Ratios

Asset Turnover (x) 1.3 1.1 1.1 1.2 1.3 1.2 1.3 1.3 Fixed Asset Turnover (x) 2.6 2.2 2.2 2.3 2.7 2.6 2.6 2.9 Debtor (Days) 60 60 54 56 66 66 66 66 Inventory (Days) 64 76 70 69 65 67 68 65 Working Capital T/O (Days) 69 76 86 72 79 73 82 81

Leverage Ratio (x)

Debt/Equity 0.4 0.9 1.0 0.7 0.6 0.4 0.3 0.2 E: MOSL Estimates

Cash Flow Statement (INR Million) Y/E March 2011 2012 2013 2014 2015 2016E 2017E 2018E Oper. Profit/(Loss) bef.Tax 10,262 10,838 11,252 12,001 17,841 22,364 23,414 32,023 Interest/Dividends Recd. 131 -107 -55 786 554 1,719 1,267 1,985 Direct Taxes Paid -1,064 -1,130 -1,188 -1,060 -2,594 -5,676 -5,655 -8,114 (Inc)/Dec in WC -2,067 -2,156 -4,088 752 -4,566 -684 -5,670 -4,269 CF from Operations 7,262 7,445 5,921 12,480 11,235 17,722 13,355 21,625 EO Expense / (Income) 0 0 0 172 84 -429 0 0 CF from Operating incl EO Exp. 7,262 7,445 5,921 12,308 11,151 18,151 13,355 21,625

(inc)/dec in FA -4,579 -12,261 -6,141 -4,553 -4,221 -6,202 -6,039 -6,000 Free Cash Flow 2,683 -4,816 -220 7,755 6,931 11,949 7,317 15,625 (Pur)/Sale of Investments 0 -35 -903 279 -678 0 0 0 CF from Investments -4,579 -12,296 -7,044 -4,274 -4,899 -6,202 -6,039 -6,000

Change in Networth -401 -945 -1,086 -1,152 -1,154 -395 -415 -436 Inc/(Dec) in Debt 406 10,508 6,928 -3,741 52 -1,105 -2,085 -1,564 Interest Paid -699 -1,211 -1,262 -1,181 -613 -452 -412 -367 Dividend Paid -1,530 -1,845 -2,105 -2,266 -2,952 -3,690 -4,428 -4,428 Others -132 58 -180 -44 -374 0 0 0 CF from Fin. Activity -2,356 6,565 2,294 -8,384 -5,041 -5,642 -7,340 -6,795

Inc/Dec of Cash 326 1,714 1,172 -350 1,211 6,307 -23 8,831 Add: Beginning Balance 2,507 2,952 4,666 5,838 5,488 6,699 13,006 12,982 Closing Balance 2,833 4,666 5,838 5,488 6,699 13,006 12,983 21,813 E: MOSL Estimates

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Corporate profile: Cadila Healthcare

Exhibit 13: Shareholding pattern (%) Sep-15 Jun-15 Sep-14

Promoter 74.8 74.8 74.8

DII 8.4 8.0 8.1

FII 6.7 7.0 6.4

Others 10.1 10.2 10.7

Note: FII Includes depository receipts

Exhibit 14: Top holders Holder Name % Holding

Life Insurance Corporation of India Ltd 3.0 Government Pension Fund Global 1.1

Exhibit 15: Top management Name Designation

Pankaj R Patel Chairman & Managing Director

Sharvil P Patel Deputy Managing Director

Exhibit 16: Directors Name Name

Pankaj R Patel Mukesh M Patel*

Sharvil P Patel Nitin Raojibhai Desai*

H Dhanrajgir* Dharmishta N Rawal*

*Independent

Exhibit 17: Auditors

Name Type

Mukesh M Shah & Co Statutory Dalwadi & Associates Cost Auditor

Exhibit 18: MOSL forecast v/s consensus EPS

(INR) MOSL

forecast Consensus

forecast Variation

(%) FY16 15.1 14.9 1.3 FY17 14.5 18.4 -21.2 FY18 21.0 22.6 -7.2

Company description Cadila is one of the largest domestic pharma companies in India with a strong focus on the global generics opportunity. The company is gradually building its presence in the regulated generic markets beginning with the US and France. It also plans to tap some unique opportunities through its JVs with Takeda, Hospira, Bayer and Bharat Serums.

Exhibit 12: Sensex rebased

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N O T E S

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Disclosure of Interest Statement Cadila Health Analyst ownership of the stock No Served as an officer, director or employee No

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