FDA NDC Directory · JSON-LD · Markdown

ATONCY

NDC 30698-456 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameAtomoxetine hydrochloride
Labeler / ManufacturerValidus Pharmaceuticals LLC
Marketing categoryNew Drug Application (innovator) · App NDA220320
Dosage form / routeSOLUTION · ORAL
Active ingredientsATOMOXETINE HYDROCHLORIDE (4 mg/mL)
Marketing started20260320
Package count1

External sources

Source: openFDA. Public-domain (CC0).