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Pantoprazole Sodium - 50268-636-15 - (Pantoprazole Sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 50268-636
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: 50268-636
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078281
Marketing Category: ANDA
Start Marketing Date: 20130115

Package Information of Pantoprazole Sodium

Package NDC: 50268-636-15
Package Description: 50 TABLET, DELAYED RELEASE in 1 BOX, UNIT-DOSE (50268-636-15)

NDC Information of Pantoprazole Sodium

NDC Code 50268-636-15
Proprietary Name Pantoprazole Sodium
Package Description 50 TABLET, DELAYED RELEASE in 1 BOX, UNIT-DOSE (50268-636-15)
Product NDC 50268-636
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130115
Marketing Category Name ANDA
Labeler Name AvPAK
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


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