FDA NDC Directory · JSON-LD · Markdown

PAROXETINE

NDC 0904-5677 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameparoxetine hydrochloride
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA075356
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE ANHYDROUS (20 mg/1)
Marketing started20030908
Package count1

External sources

Source: openFDA. Public-domain (CC0).