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Paroxetine

NDC 55289-972 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077584
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (20 mg/1)
Marketing started20070413
Package count3

External sources

Source: openFDA. Public-domain (CC0).