FDA NDC Directory · JSON-LD · Markdown

FLUOXETINE

NDC 64380-903 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namefluoxetine
Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA212684
Dosage form / routeTABLET · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20240812
Package count2

External sources

Source: openFDA. Public-domain (CC0).