FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 59651-899 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20250711
Package count4

External sources

Source: openFDA. Public-domain (CC0).