Alembic Pharmaceuticals receives USFDA final approval for Bimatoprost Ophthalmic Solution
Capital MarketAlembic Pharmaceuticals has received final approval from the US Food & Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) Bimatoprost Ophthalmic Solution, 0.03%. The approved
ANDA is therapeutically equivalent to the reference listed drug product (RLD) Latisse Ophthalmic Solution, 0.03%, of Allergan, Inc. (Allergan). Bimatoprost Ophthalmic Solution, 0.03% is indicated to treat hypotrichosis of the eyelashes by increasing their growth including length, thickness and darkness.
Bimatoprost Ophthalmic Solution, 0.03% has an estimated market size of US$ 57
million for twelve months ending September 2019 according to IQVIA.
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