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Pantoprazole Sodium - 49349-809-02 - (Pantoprazole Sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 49349-809
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: 49349-809
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091231
Marketing Category: ANDA
Start Marketing Date: 20111115

Package Information of Pantoprazole Sodium

Package NDC: 49349-809-02
Package Description: 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-809-02)

NDC Information of Pantoprazole Sodium

NDC Code 49349-809-02
Proprietary Name Pantoprazole Sodium
Package Description 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (49349-809-02)
Product NDC 49349-809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20111115
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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