FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 68071-2375 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204597
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20150316
Package count2

External sources

Source: openFDA. Public-domain (CC0).