"0051-3046-16" National Drug Code (NDC)

NDC Code	0051-3046-16
Package Description	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0051-3046-16)
Product NDC	0051-3046
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lansoprazole
Non-Proprietary Name	Lansoprazole
Dosage Form	CAPSULE, DELAYED RELEASE
Usage	ORAL
Start Marketing Date	19950510
End Marketing Date	20210228
Marketing Category Name	APPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Application Number	NDA020406
Manufacturer	AbbVie Inc.
Substance Name	LANSOPRAZOLE
Strength	30
Strength Unit	mg/1
Pharmacy Classes	Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Inhibition Gastric Acid Secretion [PE]