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