| NDC Code | 71288-022-11 |
|---|
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (71288-022-11) / 10 mL in 1 VIAL, SINGLE-DOSE (71288-022-10) |
|---|
| Product NDC | 71288-022 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Vancomycin Hydrochloride |
|---|
| Non-Proprietary Name | Vancomycin Hydrochloride |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20220728 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA215197 |
|---|
| Manufacturer | Meitheal Pharmaceuticals Inc. |
|---|
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/10mL |
|---|
| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
|---|