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DULOXETINE HYDROCHLORIDE

NDC 62332-280 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameDuloxetine
Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202949
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (60 mg/1)
Marketing started20260409
Package count3

External sources

Source: openFDA. Public-domain (CC0).