NDC 0259-1620 – Xeomin

Botulinum Toxin Type A 200 [USP'U]/1 · Injection, Powder, Lyophilized, For Solution · Intramuscular

Human Prescription Drug

Product NDC0259-1620

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
November 20, 2015
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 (2)

Package NDCDescriptionSince
0259-1620-011 VIAL, SINGLE-USE in 1 CARTON (0259-1620-01) / 200 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USENov 20, 2015
0259-1620-101 VIAL, SINGLE-USE in 1 CARTON (0259-1620-10) / 200 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USENov 20, 2015

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