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Cefuroxime axetil - 67877-215-20 - (Cefuroxime axetil)

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Drug Information of Cefuroxime axetil

Product NDC: 67877-215
Proprietary Name: Cefuroxime axetil
Non Proprietary Name: Cefuroxime axetil
Active Ingredient(s): 250    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: 67877-215
Labeler Name: Ascend Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065496
Marketing Category: ANDA
Start Marketing Date: 20101201

Package Information of Cefuroxime axetil

Package NDC: 67877-215-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (67877-215-20)

NDC Information of Cefuroxime axetil

NDC Code 67877-215-20
Proprietary Name Cefuroxime axetil
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (67877-215-20)
Product NDC 67877-215
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefuroxime axetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101201
Marketing Category Name ANDA
Labeler Name Ascend Laboratories, LLC
Substance Name CEFUROXIME AXETIL
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefuroxime axetil


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