FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 62332-243 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208698
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20170407
Package count3

External sources

Source: openFDA. Public-domain (CC0).