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Paroxetine

NDC 68788-7410 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077584
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20180606
Package count6

External sources

Source: openFDA. Public-domain (CC0).