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PAROXETINE

NDC 60429-736 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameparoxetine hydrochloride
Labeler / ManufacturerGolden State Medical Supply, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075356
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE ANHYDROUS (30 mg/1)
Marketing started20030730
Package count3

External sources

Source: openFDA. Public-domain (CC0).