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Jeuveau

NDC 72301-595 · HUMAN PRESCRIPTION DRUG · POWDER

Generic namePrabotulinum Toxin Type A
Labeler / ManufacturerEvolus, Inc.
Marketing categoryBiologic License Application · App BLA761085
Dosage form / routePOWDER · INTRAMUSCULAR
Active ingredientsBOTULINUM TOXIN TYPE A (100 [USP'U]/1)
Marketing started20190213
Package count1

External sources

Source: openFDA. Public-domain (CC0).