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Pantoprazole Sodium - 55154-6263-0 - (pantoprazole sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 55154-6263
Proprietary Name: Pantoprazole Sodium
Non Proprietary Name: pantoprazole sodium
Active Ingredient(s): 20    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: 55154-6263
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090970
Marketing Category: ANDA
Start Marketing Date: 20120123

Package Information of Pantoprazole Sodium

Package NDC: 55154-6263-0
Package Description: 10 POUCH in 1 BAG (55154-6263-0) > 1 TABLET, DELAYED RELEASE in 1 POUCH

NDC Information of Pantoprazole Sodium

NDC Code 55154-6263-0
Proprietary Name Pantoprazole Sodium
Package Description 10 POUCH in 1 BAG (55154-6263-0) > 1 TABLET, DELAYED RELEASE in 1 POUCH
Product NDC 55154-6263
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pantoprazole sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120123
Marketing Category Name ANDA
Labeler Name Cardinal Health
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 Sodium


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