FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 60687-659 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20220721
Package count1

External sources

Source: openFDA. Public-domain (CC0).