FDA NDC Directory · JSON-LD · Markdown

DULOXETINE DELAYED-RELEASE

NDC 63187-720 · 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 (20 mg/1)
Marketing started20140611
Package count3

External sources

Source: openFDA. Public-domain (CC0).