FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 25000-149 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameFluoxetine Hydrochloride
Labeler / ManufacturerMARKSANS PHARMA LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA075465
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20220129
Package count2

External sources

Source: openFDA. Public-domain (CC0).