"61715-151-42" National Drug Code (NDC)

NDC Code	61715-151-42
Package Description	42 BLISTER PACK in 1 CARTON (61715-151-42) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC	61715-151
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Preferred Plus Omeprazole
Non-Proprietary Name	Omeprazole
Dosage Form	TABLET, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	20141020
Marketing Category Name	NDA
Application Number	NDA022032
Manufacturer	Kinray
Substance Name	OMEPRAZOLE
Strength	20
Strength Unit	mg/1