Protonix - 54868-4786-0 - (pantoprazole sodium)

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Drug Information of Protonix

Product NDC: 54868-4786
Proprietary Name: Protonix
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 Protonix

Product NDC: 54868-4786
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020987
Marketing Category: NDA
Start Marketing Date: 20030502

Package Information of Protonix

Package NDC: 54868-4786-0
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE (54868-4786-0)

NDC Information of Protonix

NDC Code 54868-4786-0
Proprietary Name Protonix
Package Description 90 TABLET, DELAYED RELEASE in 1 BOTTLE (54868-4786-0)
Product NDC 54868-4786
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pantoprazole sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20030502
Marketing Category Name NDA
Labeler Name Physicians Total Care, 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 Protonix


General Information