Protonix - 55154-4232-0 - (pantoprazole sodium)

Alphabetical Index


Drug Information of Protonix

Product NDC: 55154-4232
Proprietary Name: Protonix
Non Proprietary Name: pantoprazole sodium
Active Ingredient(s): 40    mg/1 & nbsp;   pantoprazole sodium
Administration Route(s): ORAL
Dosage Form(s): GRANULE, DELAYED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Protonix

Product NDC: 55154-4232
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022020
Marketing Category: NDA
Start Marketing Date: 20080229

Package Information of Protonix

Package NDC: 55154-4232-0
Package Description: 10 PACKET in 1 BAG (55154-4232-0) > 40 GRANULE, DELAYED RELEASE in 1 PACKET

NDC Information of Protonix

NDC Code 55154-4232-0
Proprietary Name Protonix
Package Description 10 PACKET in 1 BAG (55154-4232-0) > 40 GRANULE, DELAYED RELEASE in 1 PACKET
Product NDC 55154-4232
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name pantoprazole sodium
Dosage Form Name GRANULE, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20080229
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