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PANTOPRAZOLE SODIUM - 35356-622-90 - (PANTOPRAZOLE SODIUM)

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Drug Information of PANTOPRAZOLE SODIUM

Product NDC: 35356-622
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: 35356-622
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091231
Marketing Category: ANDA
Start Marketing Date: 20110119

Package Information of PANTOPRAZOLE SODIUM

Package NDC: 35356-622-90
Package Description: 90 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-622-90)

NDC Information of PANTOPRAZOLE SODIUM

NDC Code 35356-622-90
Proprietary Name PANTOPRAZOLE SODIUM
Package Description 90 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-622-90)
Product NDC 35356-622
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PANTOPRAZOLE SODIUM
Dosage Form Name TABLET, DELAYED RELEASE
Route Name ORAL
Start Marketing Date 20110119
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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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