| NDC Code | 67184-1005-1 |
|---|
| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (67184-1005-1) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE |
|---|
| Product NDC | 67184-1005 |
|---|
| 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 | 20160629 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203702 |
|---|
| Manufacturer | Qilu Pharmaceutical Co., Ltd. |
|---|
| Substance Name | CEFTRIAXONE SODIUM |
|---|
| Strength | 250 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cephalosporin Antibacterial [EPC], Cephalosporins [CS] |
|---|