Aurobindo Pharma stock: Good growth in Europe may cushion downside
Analysts said given the strong European prospects and as most concerns relating to unit-IV are priced in, downside was limited for the stock
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Source: BS Research Bureau
Aurobindo Pharma continues to be under pressure on the bourses owing to the US Food and Drug Administration’s (US FDA’s) observations to its unit-IV facility at Hyderabad.
On Monday, Aurobindo confirmed that the unit has received nine observations between February 12 and February 20. As a result, some caution will prevail till complete clearance is given to the unit, even as analysts say the observations are not very serious.
The firm’s unit-IV makes injectables and accounts for a third of Aurobindo’s pending abbreviated new drug applications (ANDAs), analysts said. An ANDA contains data, which is submitted to the FDA for review and approval of a generic drug. After approval, companies can sell the generics in the US market.
Injectables, which contribute a fifth to US sales, are a key earnings driver. The US accounts for 44 per cent of Aurobindo’s sales. Injectables witness limited competition, and hence enjoy higher profit margins of over 20 per cent compared with 12-15 per cent for oral solids.
Ranvir Singh at Systematix Shares said of the addressable market of $87.2 billion highlighted by Aurobindo in its Q3 FY18 presentation, a third would be from niche products such as injectables. So, any disruption in supplies from unit-IV can have a bearing on Aurobindo’s prospects.
A positive is that analysts do not consider the observations as serious. Kotak Institutional Equities said the observations could be viewed as ‘low to moderate’ in criticality and could be addressed by Aurobindo without major remediation.
On Monday, Aurobindo confirmed that the unit has received nine observations between February 12 and February 20. As a result, some caution will prevail till complete clearance is given to the unit, even as analysts say the observations are not very serious.
The firm’s unit-IV makes injectables and accounts for a third of Aurobindo’s pending abbreviated new drug applications (ANDAs), analysts said. An ANDA contains data, which is submitted to the FDA for review and approval of a generic drug. After approval, companies can sell the generics in the US market.
Injectables, which contribute a fifth to US sales, are a key earnings driver. The US accounts for 44 per cent of Aurobindo’s sales. Injectables witness limited competition, and hence enjoy higher profit margins of over 20 per cent compared with 12-15 per cent for oral solids.
Ranvir Singh at Systematix Shares said of the addressable market of $87.2 billion highlighted by Aurobindo in its Q3 FY18 presentation, a third would be from niche products such as injectables. So, any disruption in supplies from unit-IV can have a bearing on Aurobindo’s prospects.
A positive is that analysts do not consider the observations as serious. Kotak Institutional Equities said the observations could be viewed as ‘low to moderate’ in criticality and could be addressed by Aurobindo without major remediation.
Source: BS Research Bureau