FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 16714-722 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerNorthStar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20080131
Package count3

External sources

Source: openFDA. Public-domain (CC0).