FDA NDC Directory · JSON-LD · Markdown

Paroxetine

NDC 63187-927 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameparoxetine hydrochloride hemihydrate
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203854
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (20 mg/1)
Marketing started20141101
Package count3

External sources

Source: openFDA. Public-domain (CC0).