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Wockhardt receives US FDA approval for Olopatadine HCI receives US FDA approval for Olopatadine HCI

expressbpdJuly 04, 2017

Tag: WOCKHARDT , US FDA approval , Olopatadine HCI

Wockhardt has received final approval from US FDA for its ANDA for 0.1 per cent ophthalmic solution of Olopatadine HCI. The eye drop Olopatadine HCI 0.1 per cent ophthalmic solution is a generic version of Patanol, marketed at a US by Alcon, a subsidiary of Novartis

The product will be manufactured at US FDA approved contract manufacturing organisation based in Montreal, Canada.

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