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LETYBO

NDC 81165-050 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Generic nameletibotulinumtoxinA-wlbg
Labeler / ManufacturerHugel, Inc.
Marketing categoryBiologic License Application · App BLA761225
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAMUSCULAR
Active ingredientsLETIBOTULINUMTOXINA (50 U/1)
Marketing started20240730
Package count1

External sources

Source: openFDA. Public-domain (CC0).