| NDC Code | 72960-112-01 |
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| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (72960-112-01) / 1.2 mL in 1 VIAL, SINGLE-USE |
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| Product NDC | 72960-112 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Daxxify |
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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 | 20220920 |
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| Marketing Category Name | BLA |
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| Application Number | BLA761127 |
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| Manufacturer | Revance Therapeutics, Inc. |
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| Substance Name | BOTULINUM TOXIN TYPE A |
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| Strength | 100 |
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| Strength Unit | U/1.2mL |
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| Pharmacy Classes | Acetylcholine Release Inhibitor [EPC], Acetylcholine Release Inhibitors [MoA], Neuromuscular Blockade [PE], Neuromuscular Blocker [EPC] |
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