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Lansoprazole - 55111-399-79 - (lansoprazole)

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Drug Information of Lansoprazole

Product NDC: 55111-399
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: 55111-399
Labeler Name: Dr.Reddy's Laboratories Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091269
Marketing Category: ANDA
Start Marketing Date: 20101015

Package Information of Lansoprazole

Package NDC: 55111-399-79
Package Description: 1 BLISTER PACK in 1 CARTON (55111-399-79) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Lansoprazole

NDC Code 55111-399-79
Proprietary Name Lansoprazole
Package Description 1 BLISTER PACK in 1 CARTON (55111-399-79) > 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55111-399
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lansoprazole
Dosage Form Name CAPSULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20101015
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Ltd.
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