Home > National Drug Code (NDC) > PANTOPRAZOLE SODIUM

PANTOPRAZOLE SODIUM - 50436-8102-2 - (PANTOPRAZOLE SODIUM)

Alphabetical Index


Drug Information of PANTOPRAZOLE SODIUM

Product NDC: 50436-8102
Proprietary Name: PANTOPRAZOLE SODIUM
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 PANTOPRAZOLE SODIUM

Product NDC: 50436-8102
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091231
Marketing Category: ANDA
Start Marketing Date: 20110119

Package Information of PANTOPRAZOLE SODIUM

Package NDC: 50436-8102-2
Package Description: 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50436-8102-2)

NDC Information of PANTOPRAZOLE SODIUM

NDC Code 50436-8102-2
Proprietary Name PANTOPRAZOLE SODIUM
Package Description 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50436-8102-2)
Product NDC 50436-8102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PANTOPRAZOLE SODIUM
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110119
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name PANTOPRAZOLE SODIUM
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of PANTOPRAZOLE SODIUM


General Information