FDA NDC Directory · JSON-LD · Markdown

Duloxetine

NDC 52427-913 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerAlmatica Pharma LLC
Marketing categoryNew Drug Application (innovator) · App NDA219131
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (90 mg/1)
Marketing started20260701
Package count1

External sources

Source: openFDA. Public-domain (CC0).