| NDC Code | 70518-0659-1 |
|---|
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (70518-0659-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-0659-0) |
|---|
| Product NDC | 70518-0659 |
|---|
| 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 | 20170802 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065169 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | CEFTRIAXONE SODIUM |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
|---|