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Lansoprazole - 55648-670-03 - (Lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 55648-670
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: 55648-670
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202176
Marketing Category: ANDA
Start Marketing Date: 20120810

Package Information of Lansoprazole

Package NDC: 55648-670-03
Package Description: 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55648-670-03)

NDC Information of Lansoprazole

NDC Code 55648-670-03
Proprietary Name Lansoprazole
Package Description 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55648-670-03)
Product NDC 55648-670
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120810
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
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