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BOTOX

NDC 0023-1145 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameonabotulinumtoxinA
Labeler / ManufacturerAllergan, Inc.
Marketing categoryBiologic License Application · App BLA103000
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRADERMAL INTRAMUSCULAR
Active ingredientsBOTULINUM TOXIN TYPE A (100 [USP'U]/1)
Marketing started19891215
Package count2

External sources

Source: openFDA. Public-domain (CC0).