FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 84386-106 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA213265
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (60 mg/1)
Marketing started20260115
Package count1

External sources

Source: openFDA. Public-domain (CC0).