FDA NDC Directory · JSON-LD · Markdown

Fluoxetine Hydrochloride

NDC 70954-600 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216448
Dosage form / routeSOLUTION · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/5mL)
Marketing started20221109
Package count1

External sources

Source: openFDA. Public-domain (CC0).