| NDC Code | 55390-139-10 |
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| Package Description | 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (55390-139-10) |
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| Product NDC | 55390-139 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Polymyxin B |
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| Non-Proprietary Name | Polymyxin B Sulfate |
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| Dosage Form | INJECTION, POWDER, FOR SOLUTION |
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| Usage | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
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| Start Marketing Date | 19980601 |
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| End Marketing Date | 20140331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA060716 |
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| Manufacturer | Bedford Laboratories |
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| Substance Name | POLYMYXIN B SULFATE |
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| Strength | 500000 |
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| Strength Unit | [iU]/1 |
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| Pharmacy Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient] |
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