NDC Code | 39822-0170-2 |
Package Description | 10 VIAL in 1 CARTON (39822-0170-2) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (39822-0170-1) |
Product NDC | 39822-0170 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Polymyxin B |
Non-Proprietary Name | Polymyxin B |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
Start Marketing Date | 20140115 |
Marketing Category Name | ANDA |
Application Number | ANDA202766 |
Manufacturer | X-GEN Pharmaceuticals, Inc. |
Substance Name | POLYMYXIN B SULFATE |
Strength | 500000 |
Strength Unit | [USP'U]/1 |
Pharmacy Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [CS] |