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Duloxetine Delayed-Release

NDC 82804-024 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Generic nameDULOXETINE HYDROCHLORIDE
Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA203088
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (40 mg/1)
Marketing started20180521
Package count3

External sources

Source: openFDA. Public-domain (CC0).