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fluoxetine

NDC 75834-148 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefluoxetine hydrochloride
Labeler / ManufacturerNIVAGEN PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA209695
Dosage form / routeTABLET · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (60 mg/1)
Marketing started20171211
Package count1

External sources

Source: openFDA. Public-domain (CC0).