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Fluoxetine

NDC 51655-274 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204597
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20200520
Package count1

External sources

Source: openFDA. Public-domain (CC0).