NDC 72960-112

Daxxify 100 U per 1.2 mL injection, powder, lyophilized, for solution

On the label: Revance Therapeutics, Inc..

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
PCI San Diego, Inc.San Diego, CA, United StatesMakes it Problems found, fixed voluntarilyMay 9, 2025 · 11 inspections
Revance Therapeutics, Inc.Newark, CA, United StatesMakes it, makes the active ingredient and tests it Problems found, fixed voluntarilyFeb 27, 2025 · 1 inspection
A+ Secure Packaging, LLCLa Vergne, TN, United StatesPackages it and labels it No problems foundJun 7, 2023 · 4 inspections

Product details

Generic drug
Botulinum Toxin Type A: every company that makes it
Form
injection, powder, lyophilized, for solution, intramuscular
Strength
100 U per 1.2 mL
Approval
BLA BLA761127
On the market since
Sep 20, 2022
Package NDCs
72960-112-01 72960-112-02 72960-112-05 72960-112-06
Official label
DailyMed (National Library of Medicine), updated Jan 7, 2026

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