FDA NDC Directory · JSON-LD · Markdown

FLUOXETINE

NDC 23155-030 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA201336
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20241013
Package count4

External sources

Source: openFDA. Public-domain (CC0).