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PAROXETINE

NDC 63629-9500 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namePAROXETINE HYDROCHLORIDE HEMIHYDRATE
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA209293
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (37.5 mg/1)
Marketing started20180914
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).