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Pantoprazole Sodium - 0008-0606-01 - (PANTOPRAZOLE SODIUM)

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Drug Information of Pantoprazole Sodium

Product NDC: 0008-0606
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: 0008-0606
Labeler Name: Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020987
Marketing Category: NDA
Start Marketing Date: 20080131

Package Information of Pantoprazole Sodium

Package NDC: 0008-0606-01
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0606-01)

NDC Information of Pantoprazole Sodium

NDC Code 0008-0606-01
Proprietary Name Pantoprazole Sodium
Package Description 90 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0606-01)
Product NDC 0008-0606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PANTOPRAZOLE SODIUM
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080131
Marketing Category Name NDA
Labeler Name Wyeth Pharmaceuticals Company, a subsidiary of Pfizer Inc.
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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