NDC Code | 25021-182-66 |
Package Description | 25 VIAL in 1 CARTON (25021-182-66) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL |
Product NDC | 25021-182 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Cefuroxime Sodium |
Non-Proprietary Name | Cefuroxime Sodium |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20160901 |
Marketing Category Name | ANDA |
Application Number | ANDA064125 |
Manufacturer | Sagent Pharmaceuticals |
Substance Name | CEFUROXIME SODIUM |
Strength | 750 |
Strength Unit | mg/1 |
Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |