FDA NDC Directory · JSON-LD · Markdown

Fluoxetine

NDC 42708-025 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerQPharma Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA076001
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20020129
Package count1

External sources

Source: openFDA. Public-domain (CC0).