PROTONIX - 16590-939-30 - (PANTOPRAZOLE SODIUM)

Alphabetical Index


Drug Information of PROTONIX

Product NDC: 16590-939
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: 16590-939
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020987
Marketing Category: NDA
Start Marketing Date: 20000501

Package Information of PROTONIX

Package NDC: 16590-939-30
Package Description: 30 TABLET, DELAYED RELEASE in 1 BOTTLE (16590-939-30)

NDC Information of PROTONIX

NDC Code 16590-939-30
Proprietary Name PROTONIX
Package Description 30 TABLET, DELAYED RELEASE in 1 BOTTLE (16590-939-30)
Product NDC 16590-939
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 STAT RX USA LLC
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