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Paroxetine

NDC 62332-768 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217280
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (37.5 mg/1)
Marketing started20250930
Package count2

External sources

Source: openFDA. Public-domain (CC0).