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Pantoprazole Sodium - 65862-559-99 - (Pantoprazole Sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 65862-559
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: 65862-559
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202038
Marketing Category: ANDA
Start Marketing Date: 20120928

Package Information of Pantoprazole Sodium

Package NDC: 65862-559-99
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-99)

NDC Information of Pantoprazole Sodium

NDC Code 65862-559-99
Proprietary Name Pantoprazole Sodium
Package Description 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-99)
Product NDC 65862-559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20120928
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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