"51079-007-20" National Drug Code (NDC)

NDC Code	51079-007-20
Package Description	100 BLISTER PACK in 1 CARTON (51079-007-20) > 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (51079-007-01)
Product NDC	51079-007
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Omeprazole
Non-Proprietary Name	Omeprazole
Dosage Form	CAPSULE, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20030901
Marketing Category Name	ANDA
Application Number	ANDA075876
Manufacturer	Mylan Institutional Inc.
Substance Name	OMEPRAZOLE
Strength	20
Strength Unit	mg/1
Pharmacy Classes	Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA]