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Lansoprazole - 0378-8030-05 - (lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 0378-8030
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 PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Lansoprazole

Product NDC: 0378-8030
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090763
Marketing Category: ANDA
Start Marketing Date: 20121106

Package Information of Lansoprazole

Package NDC: 0378-8030-05
Package Description: 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-05)

NDC Information of Lansoprazole

NDC Code 0378-8030-05
Proprietary Name Lansoprazole
Package Description 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-8030-05)
Product NDC 0378-8030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE PELLETS
Route Name ORAL
Start Marketing Date 20121106
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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