| NDC Code | 0259-1620-01 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0259-1620-01) / 200 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE |
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| Product NDC | 0259-1620 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Xeomin |
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| Non-Proprietary Name | Incobotulinumtoxina |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAMUSCULAR |
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| Start Marketing Date | 20151120 |
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| Marketing Category Name | BLA |
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| Application Number | BLA125360 |
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| Manufacturer | Merz Pharmaceuticals, LLC |
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| Substance Name | BOTULINUM TOXIN TYPE A |
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| Strength | 200 |
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| Strength Unit | [USP'U]/1 |
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| Pharmacy Classes | Acetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC] |
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