| NDC Code | 52125-842-01 |
|---|
| Package Description | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (52125-842-01) |
|---|
| Product NDC | 52125-842 |
|---|
| 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 | 20140220 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065169 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | CEFTRIAXONE SODIUM |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/1 |
|---|
| Pharmacy Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
|---|