| NDC Code | 0143-9941-10 |
|---|
| Package Description | 10 VIAL in 1 CARTON (0143-9941-10) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9941-01) |
|---|
| Product NDC | 0143-9941 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Polymyxin B |
|---|
| Non-Proprietary Name | Polymyxin B Sulfate |
|---|
| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
|---|
| Start Marketing Date | 19980601 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA060716 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | POLYMYXIN B SULFATE |
|---|
| Strength | 500000 |
|---|
| Strength Unit | [iU]/1 |
|---|
| Pharmacy Classes | Polymyxin-class Antibacterial [EPC], Polymyxins [CS] |
|---|