NDC Code | 60505-6152-4 |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (60505-6152-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE |
Product NDC | 60505-6152 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Ceftriaxone Sodium |
Non-Proprietary Name | Ceftriaxone Sodium |
Dosage Form | INJECTION, POWDER, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20170630 |
Marketing Category Name | ANDA |
Application Number | ANDA203702 |
Manufacturer | Apotex Corp. |
Substance Name | CEFTRIAXONE SODIUM |
Strength | 500 |
Strength Unit | mg/1 |
Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |