| NDC Code | 70436-020-82 |
|---|
| Package Description | 10 VIAL in 1 CARTON (70436-020-82) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
|---|
| Product NDC | 70436-020 |
|---|
| 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 | 20190603 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA212332 |
|---|
| Manufacturer | Slate Run Pharmaceuticals, LLC |
|---|
| Substance Name | VANCOMYCIN HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Glycopeptide Antibacterial [EPC], Glycopeptides [CS] |
|---|