NDC Code | 70860-103-10 |
Package Description | 10 VIAL in 1 CARTON (70860-103-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (70860-103-41) |
Product NDC | 70860-103 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Polymyxin B |
Non-Proprietary Name | Polymyxin B Sulfate |
Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Usage | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
Start Marketing Date | 20170101 |
Marketing Category Name | ANDA |
Application Number | ANDA207322 |
Manufacturer | Athenex Pharmaceutical Division, LLC. |
Substance Name | POLYMYXIN B SULFATE |
Strength | 500000 |
Strength Unit | [iU]/1 |
Pharmacy Classes | Polymyxin-class Antibacterial [EPC], Polymyxins [CS] |