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Paroxetine

NDC 68788-4130 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameparoxetine hydrochloride hemihydrate
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203854
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20260928
Package count5

External sources

Source: openFDA. Public-domain (CC0).