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Xeomin

NDC 46783-161 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameincobotulinumtoxinA
Labeler / ManufacturerMerz North America, Inc.
Marketing categoryBiologic License Application · App BLA125360
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR
Active ingredientsBOTULINUM TOXIN TYPE A (50 [USP'U]/1)
Marketing started20110801
Package count1

External sources

Source: openFDA. Public-domain (CC0).