NDC 46783-161
Xeomin 50 [USP'U] injection, powder, lyophilized, for solution
On the label: Merz North America, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Merz North America, Inc. names for other drugs.
Product details
- Generic drug
- Botulinum Toxin Type A: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intramuscular
- Strength
- 50 [USP'U]
- Approval
- BLA BLA125360
- On the market since
- Aug 1, 2011
- Package NDCs
46783-161-01- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2026
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