NDC 46783-161 – Xeomin

Botulinum Toxin Type A 50 [USP'U]/1 · Injection, Powder, Lyophilized, For Solution · Intramuscular

Human Prescription Drug

Product NDC46783-161

Product details

Brand name
Xeomin
Generic name
incobotulinumtoxinA
Labeler
Merz North America, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intramuscular
Marketing category
BLA · BLA125360
Marketed since
August 1, 2011
Listing expires
December 31, 2027
Pharmacologic class
Acetylcholine Release Inhibitor; Neuromuscular Blocker

Active ingredients

Uses, dosage, side effects and warnings for Xeomin →

Package NDC codes (1)

Package NDCDescriptionSince
46783-161-011 VIAL, SINGLE-USE in 1 CARTON (46783-161-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USEAug 1, 2011

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