"57237-018-90" National Drug Code (NDC)

NDC Code	57237-018-90
Package Description	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-018-90)
Product NDC	57237-018
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Duloxetine
Non-Proprietary Name	Duloxetine Hydrochloride
Dosage Form	CAPSULE, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20131211
Marketing Category Name	ANDA
Application Number	ANDA090778
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	DULOXETINE HYDROCHLORIDE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]