FDA NDC Directory · JSON-LD · Markdown

Paroxetine

NDC 43547-348 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameparoxetine hydrochloride hemihydrate
Labeler / ManufacturerSolco Healthcare US, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203854
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAROXETINE HYDROCHLORIDE HEMIHYDRATE (20 mg/1)
Marketing started20220329
Package count4

External sources

Source: openFDA. Public-domain (CC0).