FDA NDC Directory · JSON-LD · Markdown

Atomoxetine

NDC 0904-6908 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090609
Dosage form / routeCAPSULE · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20180223
Package count1

External sources

Source: openFDA. Public-domain (CC0).