| NDC Code | 45932-0028-1 |
|---|
| Package Description | 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45932-0028-1) |
|---|
| Product NDC | 45932-0028 |
|---|
| 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 | 20140410 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091377 |
|---|
| Manufacturer | Xellia Pharmaceuticals, ApS |
|---|
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Glycopeptide Antibacterial [EPC],Glycopeptides [CS] |
|---|