NDC 0259-1605 – Xeomin

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

Human Prescription Drug

Product NDC0259-1605

Product details

Brand name
Xeomin
Generic name
incobotulinumtoxinA
Labeler
Merz Pharmaceuticals, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intramuscular
Marketing category
BLA · BLA125360
Marketed since
September 1, 2010
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
0259-1605-011 VIAL, SINGLE-USE in 1 CARTON (0259-1605-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USESep 1, 2010

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