"57237-161-99" National Drug Code (NDC)

NDC Code	57237-161-99
Package Description	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-161-99)
Product NDC	57237-161
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Omeprazole
Non-Proprietary Name	Omeprazole
Dosage Form	CAPSULE, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20150819
Marketing Category Name	ANDA
Application Number	ANDA203270
Manufacturer	Rising Pharma Holdings, Inc.
Substance Name	OMEPRAZOLE
Strength	20
Strength Unit	mg/1
Pharmacy Classes	Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]