FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 0121-4721 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameFLUOXETINE HYDROCHLORIDE
Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA076015
Dosage form / routeSOLUTION · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/5mL)
Marketing started20020201
Package count1

External sources

Source: openFDA. Public-domain (CC0).