FDA NDC Directory · JSON-LD · Markdown

Duloxetine HCL DR

NDC 80425-0014 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameDuloxetine HCL
Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090778
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20221211
Package count2

External sources

Source: openFDA. Public-domain (CC0).