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Cefuroxime Axetil - 52959-939-20 - (Cefuroxime Axetil)

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Drug Information of Cefuroxime Axetil

Product NDC: 52959-939
Proprietary Name: Cefuroxime Axetil
Non Proprietary Name: Cefuroxime Axetil
Active Ingredient(s): 500    mg/1 & nbsp;   Cefuroxime Axetil
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cefuroxime Axetil

Product NDC: 52959-939
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065308
Marketing Category: ANDA
Start Marketing Date: 20060329

Package Information of Cefuroxime Axetil

Package NDC: 52959-939-20
Package Description: 20 TABLET in 1 BOTTLE (52959-939-20)

NDC Information of Cefuroxime Axetil

NDC Code 52959-939-20
Proprietary Name Cefuroxime Axetil
Package Description 20 TABLET in 1 BOTTLE (52959-939-20)
Product NDC 52959-939
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefuroxime Axetil
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060329
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name CEFUROXIME AXETIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefuroxime Axetil


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