FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 77771-114 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerRADHA PHARMACEUTICALS, INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204597
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20221024
Package count2

External sources

Source: openFDA. Public-domain (CC0).