FDA NDC Directory · JSON-LD · Markdown

FLUOXETINE

NDC 71656-089 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerSaptalis Pharmaceuticals, LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075525
Dosage form / routeSOLUTION · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/5mL)
Marketing started20250620
Package count1

External sources

Source: openFDA. Public-domain (CC0).