Cefuroxime - 44567-712-10 - (Cefuroxime)

Alphabetical Index


Drug Information of Cefuroxime

Product NDC: 44567-712
Proprietary Name: Cefuroxime
Non Proprietary Name: Cefuroxime
Active Ingredient(s): 7.5    g/80mL & nbsp;   Cefuroxime
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Cefuroxime

Product NDC: 44567-712
Labeler Name: WG Critical Care, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064124
Marketing Category: ANDA
Start Marketing Date: 20121004

Package Information of Cefuroxime

Package NDC: 44567-712-10
Package Description: 10 VIAL in 1 CARTON (44567-712-10) > 80 mL in 1 VIAL

NDC Information of Cefuroxime

NDC Code 44567-712-10
Proprietary Name Cefuroxime
Package Description 10 VIAL in 1 CARTON (44567-712-10) > 80 mL in 1 VIAL
Product NDC 44567-712
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cefuroxime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20121004
Marketing Category Name ANDA
Labeler Name WG Critical Care, LLC
Substance Name CEFUROXIME SODIUM
Strength Number 7.5
Strength Unit g/80mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of Cefuroxime


General Information