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Polymyxin B
Polymyxin B - 55390-139-10 - (Polymyxin B sulfate)
Drug Information of Polymyxin B
| Product NDC: | 55390-139 |
| Proprietary Name: | Polymyxin B |
| Non Proprietary Name: | Polymyxin B sulfate |
| Active Ingredient(s): | 500000 [iU]/300mL & nbsp; Polymyxin B sulfate |
| Administration Route(s): | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Polymyxin B
| Product NDC: | 55390-139 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA060716 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19980601 |
Package Information of Polymyxin B
| Package NDC: | 55390-139-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-139-10) > 300 mL in 1 VIAL |
NDC Information of Polymyxin B
| NDC Code | 55390-139-10 |
| Proprietary Name | Polymyxin B |
| Package Description | 10 VIAL in 1 BOX (55390-139-10) > 300 mL in 1 VIAL |
| Product NDC | 55390-139 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Polymyxin B sulfate |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
| Start Marketing Date | 19980601 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | POLYMYXIN B SULFATE |
| Strength Number | 500000 |
| Strength Unit | [iU]/300mL |
| Pharmaceutical Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
