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Cefuroxime Axetil - 64679-922-02 - (Cefuroxime Axetil)

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Drug Information of Cefuroxime Axetil

Product NDC: 64679-922
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cefuroxime Axetil

Product NDC: 64679-922
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065166
Marketing Category: ANDA
Start Marketing Date: 20050729

Package Information of Cefuroxime Axetil

Package NDC: 64679-922-02
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (64679-922-02)

NDC Information of Cefuroxime Axetil

NDC Code 64679-922-02
Proprietary Name Cefuroxime Axetil
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (64679-922-02)
Product NDC 64679-922
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefuroxime Axetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050729
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
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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