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Pantoprazole Sodium - 59746-283-03 - (Pantoprazole Sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 59746-283
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: 59746-283
Labeler Name: Jubilant Cadista Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090901
Marketing Category: ANDA
Start Marketing Date: 20110901

Package Information of Pantoprazole Sodium

Package NDC: 59746-283-03
Package Description: 10 BLISTER PACK in 1 CARTON (59746-283-03) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK

NDC Information of Pantoprazole Sodium

NDC Code 59746-283-03
Proprietary Name Pantoprazole Sodium
Package Description 10 BLISTER PACK in 1 CARTON (59746-283-03) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
Product NDC 59746-283
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals 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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