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Duloxetine

NDC 70518-1139 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA208706
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsDULOXETINE HYDROCHLORIDE (20 mg/1)
Marketing started20180425
Package count5

External sources

Source: openFDA. Public-domain (CC0).