FDA NDC Directory · JSON-LD · Markdown

Fluphenazine Hydrochloride

NDC 68462-338 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA216350
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUPHENAZINE HYDROCHLORIDE (10 mg/1)
Marketing started20231106
Package count3

External sources

Source: openFDA. Public-domain (CC0).