ZINACEF - 0173-0425-00 - (cefuroxime)

Alphabetical Index


Drug Information of ZINACEF

Product NDC: 0173-0425
Proprietary Name: ZINACEF
Non Proprietary Name: cefuroxime
Active Ingredient(s): 1.5    g/50mL & nbsp;   cefuroxime
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of ZINACEF

Product NDC: 0173-0425
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050643
Marketing Category: NDA
Start Marketing Date: 19890501

Package Information of ZINACEF

Package NDC: 0173-0425-00
Package Description: 24 CONTAINER in 1 CARTON (0173-0425-00) > 50 mL in 1 CONTAINER

NDC Information of ZINACEF

NDC Code 0173-0425-00
Proprietary Name ZINACEF
Package Description 24 CONTAINER in 1 CARTON (0173-0425-00) > 50 mL in 1 CONTAINER
Product NDC 0173-0425
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefuroxime
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19890501
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name CEFUROXIME SODIUM
Strength Number 1.5
Strength Unit g/50mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of ZINACEF


General Information