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Lansoprazole - 63739-574-10 - (lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 63739-574
Proprietary Name: Lansoprazole
Non Proprietary Name: lansoprazole
Active Ingredient(s): 15    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: 63739-574
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091269
Marketing Category: ANDA
Start Marketing Date: 20120921

Package Information of Lansoprazole

Package NDC: 63739-574-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-574-10) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Lansoprazole

NDC Code 63739-574-10
Proprietary Name Lansoprazole
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-574-10) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 63739-574
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120921
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name LANSOPRAZOLE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Lansoprazole


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