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PANTOPRAZOLE SODIUM - 68084-283-01 - (PANTOPRAZOLE SODIUM)

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Drug Information of PANTOPRAZOLE SODIUM

Product NDC: 68084-283
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: 68084-283
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077058
Marketing Category: ANDA
Start Marketing Date: 20110207

Package Information of PANTOPRAZOLE SODIUM

Package NDC: 68084-283-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-283-01) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-283-11)

NDC Information of PANTOPRAZOLE SODIUM

NDC Code 68084-283-01
Proprietary Name PANTOPRAZOLE SODIUM
Package Description 10 BLISTER PACK in 1 CARTON (68084-283-01) > 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-283-11)
Product NDC 68084-283
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PANTOPRAZOLE SODIUM
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110207
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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