ZINACEF - 0173-0354-10 - (cefuroxime)

Alphabetical Index


Drug Information of ZINACEF

Product NDC: 0173-0354
Proprietary Name: ZINACEF
Non Proprietary Name: cefuroxime
Active Ingredient(s): 1.5    g/16mL & nbsp;   cefuroxime
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ZINACEF

Product NDC: 0173-0354
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050558
Marketing Category: NDA
Start Marketing Date: 20041213

Package Information of ZINACEF

Package NDC: 0173-0354-10
Package Description: 10 VIAL in 1 TRAY (0173-0354-10) > 16 mL in 1 VIAL

NDC Information of ZINACEF

NDC Code 0173-0354-10
Proprietary Name ZINACEF
Package Description 10 VIAL in 1 TRAY (0173-0354-10) > 16 mL in 1 VIAL
Product NDC 0173-0354
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefuroxime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20041213
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name CEFUROXIME SODIUM
Strength Number 1.5
Strength Unit g/16mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of ZINACEF


General Information