FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 72241-009 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerModavar Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA206993
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20210908
Package count3

External sources

Source: openFDA. Public-domain (CC0).