FDA NDC Directory · JSON-LD · Markdown

Strattera

NDC 0002-3239 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameAtomoxetine hydrochloride
Labeler / ManufacturerEli Lilly and Company
Marketing categoryNew Drug Application (innovator) · App NDA021411
Dosage form / routeCAPSULE · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (60 mg/1)
Marketing started20021126
Marketing ended20270731
Package count1

External sources

Source: openFDA. Public-domain (CC0).