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paroxetine hydrochloride

NDC 69584-673 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerOxford Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076968
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20221114
Package count5

External sources

Source: openFDA. Public-domain (CC0).