FDA NDC Directory · JSON-LD · Markdown

Atomoxetine

NDC 31722-720 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202682
Dosage form / routeCAPSULE · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (100 mg/1)
Marketing started20210311
Package count1

External sources

Source: openFDA. Public-domain (CC0).