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“The company has received final approval from the US Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) Vilazodone Hydrochloride tablets, 10 mg, 20 mg, and 40 mg,” Alembic said in a filing to BSE.
Vilazodone hydrochloride tablets are indicated for the treatment of major depressive disorder.
“The approved ANDA is therapeutically equivalent to the reference listed drug product (RLD), Viibryd tablets, 10 mg, 20 mg, and 40 mg, of Allergan Sales,” the drug firm said.
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Alembic had previously received tentative approval for this ANDA.
“Alembic was one of the first ANDA applicants to submit a substantially complete ANDA with a paragraph IV certification and hence is eligible for 180 days of shared exclusivity,” it said.
The launch of the product will be as per settlement agreement with US-based pharmaceutical firm Allergan.