| NDC Code | 51991-939-17 |
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| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (51991-939-17) > 1 INJECTION, SOLUTION in 1 VIAL, SINGLE-USE (51991-939-99) |
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| Product NDC | 51991-939 |
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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 |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC |
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| Start Marketing Date | 20160601 |
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| End Marketing Date | 20190331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA207322 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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| Substance Name | POLYMYXIN B SULFATE |
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| Strength | 500000 |
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| Strength Unit | 1/1 |
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| Pharmacy Classes | Polymyxin-class Antibacterial [EPC],Polymyxins [CS] |
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