FDA NDC Directory · JSON-LD · Markdown

Paroxetine

NDC 68084-044 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA077584
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE (10 mg/1)
Marketing started20050315
Package count2

External sources

Source: openFDA. Public-domain (CC0).