FDA NDC Directory · JSON-LD · Markdown

PAROXETINE

NDC 61919-513 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA077584
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (40 mg/1)
Marketing started20160229
Package count1

External sources

Source: openFDA. Public-domain (CC0).