FDA NDC Directory · JSON-LD · Markdown

Duloxetine

NDC 71205-445 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203197
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20120501
Package count3

External sources

Source: openFDA. Public-domain (CC0).