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Paroxetine

NDC 67046-0846 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077584
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (30 mg/1)
Marketing started20260821
Package count1

External sources

Source: openFDA. Public-domain (CC0).