FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 87441-031 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerUnit Dose Solutions, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20260622
Package count1

External sources

Source: openFDA. Public-domain (CC0).