FDA NDC Directory · JSON-LD · Markdown

Duloxetine D/R

NDC 72189-661 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA208706
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20260209
Package count2

External sources

Source: openFDA. Public-domain (CC0).