FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 65862-192 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (10 mg/1)
Marketing started20080131
Marketing ended20280229
Package count2

External sources

Source: openFDA. Public-domain (CC0).