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Paroxetine

NDC 69367-336 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213485
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (25 mg/1)
Marketing started20210726
Package count1

External sources

Source: openFDA. Public-domain (CC0).