The approval has also boosted confidence in the company’s injectables portfolio and its US business. Concerns over pricing pressure in the US and FDA inspections at its various manufacturing units had pushed down its stock to 52-week lows in early June. With FDA clearance to its Unit-IV (manufactures injectables) and product approval from its penem injectables facility, Aurobindo’s prospects are looking better, say analysts.
The approved product (Ertapenem) is the generic version of Merck’s $387 million per annum brand. Assuming 60 per cent price erosion and 25 per cent market share, it could be $45-50 million revenue opportunity for Aurobindo in FY19, estimate analysts. Being a limited-competition complex product, its contribution to top line and profits will sustain for a longer period. With plans for three more penem launches, the Street is hopeful on Aurobindo.
Analysts at Elara Capital say Ertapenem approval gives comfort to Aurobindo’s ability to grow its US business in FY19, despite the high base. The clearance for Unit-IV should bolster new injectables launches and improve product supplies from the second half of FY19, add analysts.
Reliance Securities expects Aurobindo’s US business to clock 11 per cent compounded growth over FY18-20. While US (over 40 per cent of revenue) prospects are improving, the European business is not far behind. Europe, which contributes more than a fourth to its revenue, is also seeing a margin improvement. While all these should enhance Aurobindo’s earnings, a weak rupee will only add to its kitty.
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