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Pantoprazole SodiumDelayed-Release - 43063-261-30 - (pantoprazole sodium)

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Drug Information of Pantoprazole SodiumDelayed-Release

Product NDC: 43063-261
Proprietary Name: Pantoprazole SodiumDelayed-Release
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 SodiumDelayed-Release

Product NDC: 43063-261
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020987
Marketing Category: NDA
Start Marketing Date: 20080131

Package Information of Pantoprazole SodiumDelayed-Release

Package NDC: 43063-261-30
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-261-30)

NDC Information of Pantoprazole SodiumDelayed-Release

NDC Code 43063-261-30
Proprietary Name Pantoprazole SodiumDelayed-Release
Package Description 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-261-30)
Product NDC 43063-261
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 PD-Rx 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 SodiumDelayed-Release


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