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See the DrugPatentWatch profile for daxxify
Revance’s Daxxify (daxibotulinumtoxinA-lanm) was approved by the U.S. FDA in September 2022, but the provided sources do not state the specific U.S. commercial launch date (the first date it began routine sales/availability). [1][2]
The timeline that is confirmed is FDA approval in September 2022. After approval, companies can take additional time for manufacturing ramp-up, distribution, and readiness of prescribing/administrative channels; those “go-live” details are not included in the provided information. [1][2]
You can cite the FDA approval month/year: September 2022. The exact “launch date” (day/month when product became commercially available) is not provided in the supplied material. [1][2] Sources: [1] https://www.fda.gov/news-events/press-announcements/fda-approves-daxxify-daxibotulinumtoxina-lanm-treatment-adults [2] https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=215854
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