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Fluoxetine

NDC 54838-523 · HUMAN PRESCRIPTION DRUG · LIQUID

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077849
Dosage form / routeLIQUID · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/5mL)
Marketing started20090827
Package count1

External sources

Source: openFDA. Public-domain (CC0).