Strength
100 [USP'U]/1
Manufacturer
Allergan, Inc.NDC
00023114501
Classification
Brand
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRADERMAL; INTRAMUSCULAR
Last Updated
7/5/2017
Active Ingredients
BOTULINUM TOXIN TYPE AApproval Type
Biologic (BLA)
FDA Application
BLA103000On Market Since
12/15/1989
Pharmacological Classes
Acetylcholine Release Inhibitor
Acetylcholine Release Inhibitors
Neuromuscular Blockade
Neuromuscular Blocker
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