Cefuroxime - 44567-710-10 - (Cefuroxime)

Alphabetical Index


Drug Information of Cefuroxime

Product NDC: 44567-710
Proprietary Name: Cefuroxime
Non Proprietary Name: Cefuroxime
Active Ingredient(s): 750    mg/1 & nbsp;   Cefuroxime
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefuroxime

Product NDC: 44567-710
Labeler Name: WG Critical Care, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064125
Marketing Category: ANDA
Start Marketing Date: 20121004

Package Information of Cefuroxime

Package NDC: 44567-710-10
Package Description: 10 VIAL in 1 CARTON (44567-710-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL

NDC Information of Cefuroxime

NDC Code 44567-710-10
Proprietary Name Cefuroxime
Package Description 10 VIAL in 1 CARTON (44567-710-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product NDC 44567-710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefuroxime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20121004
Marketing Category Name ANDA
Labeler Name WG Critical Care, LLC
Substance Name CEFUROXIME SODIUM
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefuroxime


General Information