CEFTIN - 0173-0741-10 - (cefuroxime axetil)

Alphabetical Index


Drug Information of CEFTIN

Product NDC: 0173-0741
Proprietary Name: CEFTIN
Non Proprietary Name: cefuroxime axetil
Active Ingredient(s): 250    mg/5mL & nbsp;   cefuroxime axetil
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of CEFTIN

Product NDC: 0173-0741
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050672
Marketing Category: NDA
Start Marketing Date: 20040602

Package Information of CEFTIN

Package NDC: 0173-0741-10
Package Description: 50 mL in 1 BOTTLE, GLASS (0173-0741-10)

NDC Information of CEFTIN

NDC Code 0173-0741-10
Proprietary Name CEFTIN
Package Description 50 mL in 1 BOTTLE, GLASS (0173-0741-10)
Product NDC 0173-0741
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefuroxime axetil
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20040602
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name CEFUROXIME AXETIL
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of CEFTIN


General Information