| NDC Code | 71288-029-12 |
|---|
| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-029-12) / 5 mL in 1 VIAL, SINGLE-DOSE (71288-029-10) |
|---|
| Product NDC | 71288-029 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Micafungin |
|---|
| Non-Proprietary Name | Micafungin Sodium |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20220928 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA215381 |
|---|
| Manufacturer | Meitheal Pharmaceuticals Inc. |
|---|
| Substance Name | MICAFUNGIN SODIUM |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/5mL |
|---|
| Pharmacy Classes | Echinocandin Antifungal [EPC], Lipopeptides [CS] |
|---|