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Sun Pharma sinks 7% on warning letter but analysts bullish

However, most analysts are still bullish on the stock and are keenly waiting to for more details in the warning letter. Few analysts have lowered target price with a cautious outlook. Phillip Capital remains positive and advises to buy on dips stating that the issue may have more sentimental impact.

December 21, 2015 / 13:19 IST
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Moneycontrol BureauShares of Sun Pharma slumped over 7 percent intraday on Monday as investors grow cautious about a warning letter for its Halol manufacturing unit. The drug major has received a warning letter from the USFDA over violation of manufacturing norms in its facility at Halol in Gujarat. The warning letter follows inspection of the facility in September 2014 by US Food and Drug Administration (USFDA) inspectors.However, most analysts are still bullish on the stock and are keenly waiting to for more details in the warning letter. Few analysts have lowered target price with a cautious outlook. Phillip Capital remains positive and advises to buy on dips stating that the issue may have more sentimental impact. It also adds that content of the warning letter will be key to future action in Sun Pharma, else it does not expect any major sales or margin implication.

The brokerage is pinning hopes on its anti-cancer drug Gleevec generic. It feels that timely Gleevec launch could surprise positively and except Gleevec there are no key injectable in near-term pipeline. "It has enough time to go for site transfer for other drugs," Phillip Cap adds.

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Sun Pharma's subsidiary received final approval from the US Food and Drug Administration (USFDA) for abbreviated new drug application (ANDA) for generic version of Gleevec, imatinib mesylate tablets 100mg and 400mg. CLSA says any weakness in Sun Pharma should be used as a buying opportunity but slashed target price per share. It feels that warning letter has a low probability of an import alert and expects earnings growth recovery from Q3FY16.

Retaining a buy rating, JM Financial sees the warning letter limited downside risk to its FY17 estimates. It has set a 14-15 percent growth estimate including Gleevec generic exclusivity. It also adds that reliance on Halol is limited to FY18 injectible filings.