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Duloxetine HCL DR

NDC 80425-0012 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameDuloxetine HCL
Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203197
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20120501
Package count2

External sources

Source: openFDA. Public-domain (CC0).