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Fluoxetine Hydrochloride

NDC 46708-242 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208698
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (10 mg/1)
Marketing started20170415
Package count3

External sources

Source: openFDA. Public-domain (CC0).