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lansoprazole - 63629-4151-1 - (lansoprazole)

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Drug Information of lansoprazole

Product NDC: 63629-4151
Proprietary Name: lansoprazole
Non Proprietary Name: lansoprazole
Active Ingredient(s): 30    mg/1 & nbsp;   lansoprazole
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of lansoprazole

Product NDC: 63629-4151
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020406
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20091111

Package Information of lansoprazole

Package NDC: 63629-4151-1
Package Description: 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63629-4151-1)

NDC Information of lansoprazole

NDC Code 63629-4151-1
Proprietary Name lansoprazole
Package Description 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63629-4151-1)
Product NDC 63629-4151
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20091111
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Bryant Ranch Prepack
Substance Name LANSOPRAZOLE
Strength Number 30
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of lansoprazole


General Information