| NDC Code | 70069-830-01 |
|---|
| Package Description | 1 VIAL in 1 CARTON (70069-830-01) / 25 mL in 1 VIAL |
|---|
| Product NDC | 70069-830 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dalbavancin |
|---|
| Non-Proprietary Name | Dalbavancin |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20260727 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA219604 |
|---|
| Manufacturer | Somerset Therapeutics, LLC |
|---|
| Substance Name | DALBAVANCIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/25mL |
|---|
| Pharmacy Classes | Lipoglycopeptide Antibacterial [EPC], Lipoglycopeptides [CS] |
|---|