FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 43063-839 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090223
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20160129
Package count2

External sources

Source: openFDA. Public-domain (CC0).