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Lansoprazole - 0781-2147-31 - (Lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 0781-2147
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: 0781-2147
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090331
Marketing Category: ANDA
Start Marketing Date: 20100423

Package Information of Lansoprazole

Package NDC: 0781-2147-31
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2147-31)

NDC Information of Lansoprazole

NDC Code 0781-2147-31
Proprietary Name Lansoprazole
Package Description 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0781-2147-31)
Product NDC 0781-2147
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20100423
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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