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PANTOPRAZOLE SODIUM - 17478-069-14 - (PANTOPRAZOLE SODIUM)

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Drug Information of PANTOPRAZOLE SODIUM

Product NDC: 17478-069
Proprietary Name: PANTOPRAZOLE SODIUM
Non Proprietary Name: PANTOPRAZOLE SODIUM
Active Ingredient(s): 40    mg/1 & nbsp;   PANTOPRAZOLE SODIUM
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of PANTOPRAZOLE SODIUM

Product NDC: 17478-069
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079197
Marketing Category: ANDA
Start Marketing Date: 20121108

Package Information of PANTOPRAZOLE SODIUM

Package NDC: 17478-069-14
Package Description: 1 VIAL in 1 CARTON (17478-069-14) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of PANTOPRAZOLE SODIUM

NDC Code 17478-069-14
Proprietary Name PANTOPRAZOLE SODIUM
Package Description 1 VIAL in 1 CARTON (17478-069-14) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 17478-069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name PANTOPRAZOLE SODIUM
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20121108
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
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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