NDC 0023-9232
BOTOX Cosmetic
Onabotulinumtoxina
BOTOX Cosmetic is a Intramuscular Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category.  It is labeled and distributed by Allergan, Inc.. The primary component is Botulinum Toxin Type A.
| Product ID | 0023-9232_03473e87-ca9a-41fc-8f37-ae44eaf50635 | 
| NDC | 0023-9232 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | BOTOX Cosmetic | 
| Generic Name | Onabotulinumtoxina | 
| Dosage Form | Injection, Powder, Lyophilized, For Solution | 
| Route of Administration | INTRAMUSCULAR | 
| Marketing Start Date | 2008-05-20 | 
| Marketing Category | BLA / BLA | 
| Application Number | BLA103000 | 
| Labeler Name | Allergan, Inc. | 
| Substance Name | BOTULINUM TOXIN TYPE A | 
| Active Ingredient Strength | 100 [USP'U]/1 | 
| Pharm Classes | Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2022-12-31 |