FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 68999-730 · HUMAN PRESCRIPTION DRUG · LIQUID

Labeler / ManufacturerChartwell Governmental & Specialty RX, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076458
Dosage form / routeLIQUID · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/5mL)
Marketing started20040514
Package count1

External sources

Source: openFDA. Public-domain (CC0).