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Lansoprazole - 52125-149-02 - (lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 52125-149
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: 52125-149
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091269
Marketing Category: ANDA
Start Marketing Date: 20130326

Package Information of Lansoprazole

Package NDC: 52125-149-02
Package Description: 30 CAPSULE, DELAYED RELEASE in 1 VIAL (52125-149-02)

NDC Information of Lansoprazole

NDC Code 52125-149-02
Proprietary Name Lansoprazole
Package Description 30 CAPSULE, DELAYED RELEASE in 1 VIAL (52125-149-02)
Product NDC 52125-149
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130326
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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