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Pantoprazole Sodium - 62175-181-43 - (Pantoprazole Sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 62175-181
Proprietary Name: Pantoprazole Sodium
Non Proprietary Name: Pantoprazole Sodium
Active Ingredient(s): 40    mg/1 & nbsp;   Pantoprazole Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Pantoprazole Sodium

Product NDC: 62175-181
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078281
Marketing Category: ANDA
Start Marketing Date: 20110120

Package Information of Pantoprazole Sodium

Package NDC: 62175-181-43
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-181-43)

NDC Information of Pantoprazole Sodium

NDC Code 62175-181-43
Proprietary Name Pantoprazole Sodium
Package Description 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-181-43)
Product NDC 62175-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110120
Marketing Category Name ANDA
Labeler Name Kremers Urban Pharmaceuticals Inc.
Substance Name PANTOPRAZOLE SODIUM
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Pantoprazole Sodium


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