FDA NDC Directory · JSON-LD · Markdown

fluoxetine hydrochloride

NDC 72162-1495 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA203836
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20160822
Package count2

External sources

Source: openFDA. Public-domain (CC0).