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Fluoxetine

NDC 59651-309 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213286
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20200408
Package count2

External sources

Source: openFDA. Public-domain (CC0).