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PAROXETINE

NDC 68180-646 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204134
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (25 mg/1)
Marketing started20170306
Package count1

External sources

Source: openFDA. Public-domain (CC0).