| NDC Code | 60492-0075-4 |
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| Package Description | 1 VIAL, GLASS in 1 CARTON (60492-0075-4) / 50 mL in 1 VIAL, GLASS (60492-0075-1) |
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| Product NDC | 60492-0075 |
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| Product Type Name | PLASMA DERIVATIVE |
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| Proprietary Name | Bat |
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| Non-Proprietary Name | Botulism Antitoxin Heptavalent |
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| Dosage Form | LIQUID |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20130301 |
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| Marketing Category Name | BLA |
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| Application Number | BLA125462 |
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| Manufacturer | Emergent BioSolutions Canada Inc |
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| Substance Name | EQUINE BOTULINUM NEUROTOXIN A IMMUNE FAB2; EQUINE BOTULINUM NEUROTOXIN B IMMUNE FAB2; EQUINE BOTULINUM NEUROTOXIN C IMMUNE FAB2; EQUINE BOTULINUM NEUROTOXIN D IMMUNE FAB2; EQUINE BOTULINUM NEUROTOXIN E IMMUNE FAB2; EQUINE BOTULINUM NEUROTOXIN F IMMUNE FAB2; EQUINE BOTULINUM NEUROTOXIN G IMMUNE FAB2 |
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| Strength | 4500; 3300; 3000; 600; 5100; 3000; 600 |
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| Strength Unit | [iU]/10mL; [iU]/10mL; [iU]/10mL; [iU]/10mL; [iU]/10mL; [iU]/10mL; [iU]/10mL |
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