Protonix - 55154-4217-0 - (pantoprazole sodium)

Alphabetical Index


Drug Information of Protonix

Product NDC: 55154-4217
Proprietary Name: Protonix
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 Protonix

Product NDC: 55154-4217
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020987
Marketing Category: NDA
Start Marketing Date: 20000501

Package Information of Protonix

Package NDC: 55154-4217-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-4217-0) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Protonix

NDC Code 55154-4217-0
Proprietary Name Protonix
Package Description 10 BLISTER PACK in 1 BAG (55154-4217-0) > 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 55154-4217
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pantoprazole sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20000501
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name PANTOPRAZOLE SODIUM
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Protonix


General Information