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DRIZALMA SPRINKLE

NDC 47335-617 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Generic nameDuloxetine
Labeler / ManufacturerSUN PHARMACEUTICAL INDUSTRIES, INC.
Marketing categoryNew Drug Application (innovator) · App NDA212516
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20240610
Package count4

External sources

Source: openFDA. Public-domain (CC0).