FDA NDC Directory · JSON-LD · Markdown

Atomoxetine

NDC 64380-477 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA079021
Dosage form / routeCAPSULE · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (80 mg/1)
Marketing started20250701
Package count2

External sources

Source: openFDA. Public-domain (CC0).