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Pantoprazole - 55111-332-78 - (Pantoprazole)

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Drug Information of Pantoprazole

Product NDC: 55111-332
Proprietary Name: Pantoprazole
Non Proprietary Name: Pantoprazole
Active Ingredient(s): 20    mg/1 & nbsp;   Pantoprazole
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Pantoprazole

Product NDC: 55111-332
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077619
Marketing Category: ANDA
Start Marketing Date: 20110119

Package Information of Pantoprazole

Package NDC: 55111-332-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-332-78) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79)

NDC Information of Pantoprazole

NDC Code 55111-332-78
Proprietary Name Pantoprazole
Package Description 10 BLISTER PACK in 1 CARTON (55111-332-78) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-332-79)
Product NDC 55111-332
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110119
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
Substance Name PANTOPRAZOLE SODIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Pantoprazole


General Information