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Duloxetine

NDC 76420-236 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE PELLETS

Labeler / ManufacturerAsclemed USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090776
Dosage form / routeCAPSULE, DELAYED RELEASE PELLETS · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (30 mg/1)
Marketing started20131217
Package count3

External sources

Source: openFDA. Public-domain (CC0).