CEFTIN - 0173-0394-00 - (cefuroxime axetil)

Alphabetical Index


Drug Information of CEFTIN

Product NDC: 0173-0394
Proprietary Name: CEFTIN
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 CEFTIN

Product NDC: 0173-0394
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050605
Marketing Category: NDA
Start Marketing Date: 19891001

Package Information of CEFTIN

Package NDC: 0173-0394-00
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (0173-0394-00)

NDC Information of CEFTIN

NDC Code 0173-0394-00
Proprietary Name CEFTIN
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (0173-0394-00)
Product NDC 0173-0394
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefuroxime axetil
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19891001
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name CEFUROXIME AXETIL
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFTIN


General Information