ZINACEF - 24987-437-00 - (cefuroxime)

Alphabetical Index


Drug Information of ZINACEF

Product NDC: 24987-437
Proprietary Name: ZINACEF
Non Proprietary Name: cefuroxime
Active Ingredient(s): 90    mg/mL & 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: 24987-437
Labeler Name: Covis Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050558
Marketing Category: NDA
Start Marketing Date: 20130115

Package Information of ZINACEF

Package NDC: 24987-437-00
Package Description: 10 VIAL in 1 TRAY (24987-437-00) > 16 mL in 1 VIAL

NDC Information of ZINACEF

NDC Code 24987-437-00
Proprietary Name ZINACEF
Package Description 10 VIAL in 1 TRAY (24987-437-00) > 16 mL in 1 VIAL
Product NDC 24987-437
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cefuroxime
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130115
Marketing Category Name NDA
Labeler Name Covis Pharmaceuticals Inc
Substance Name CEFUROXIME SODIUM
Strength Number 90
Strength Unit mg/mL
Pharmaceutical Classes Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient]

Complete Information of ZINACEF


General Information