| NDC Code | 99207-500-01 |
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| Package Description | 1 VIAL in 1 CARTON (99207-500-01) > 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL |
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| Product NDC | 99207-500 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dysport |
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| Non-Proprietary Name | Botulinum Toxin Type A |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAMUSCULAR |
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| Start Marketing Date | 20090525 |
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| End Marketing Date | 20150331 |
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| Marketing Category Name | BLA |
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| Application Number | BLA125274 |
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| Manufacturer | Medicis Pharmaceutical Corp |
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| Substance Name | BOTULINUM TOXIN TYPE A |
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| Strength | 300 |
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| Strength Unit | [USP&apos'U]/1 |
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| Pharmacy Classes | Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] |
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