FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 72789-554 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078619
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20250711
Package count3

External sources

Source: openFDA. Public-domain (CC0).