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Pantoprazole Sodium - 68084-006-01 - (Pantoprazole Sodium)

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Drug Information of Pantoprazole Sodium

Product NDC: 68084-006
Proprietary Name: Pantoprazole Sodium
Non Proprietary Name: Pantoprazole Sodium
Active Ingredient(s): 40    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: 68084-006
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078281
Marketing Category: ANDA
Start Marketing Date: 20130515

Package Information of Pantoprazole Sodium

Package NDC: 68084-006-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-006-01) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-006-11)

NDC Information of Pantoprazole Sodium

NDC Code 68084-006-01
Proprietary Name Pantoprazole Sodium
Package Description 10 BLISTER PACK in 1 CARTON (68084-006-01) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-006-11)
Product NDC 68084-006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Pantoprazole Sodium
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20130515
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name PANTOPRAZOLE SODIUM
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]

Complete Information of Pantoprazole Sodium


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