| NDC Code: |
0023-3921 |
| Proprietary Name: |
BOTOX |
| Suffix: |
|
| Non-Proprietary Name: |
onabotulinumtoxinA |
| Dosage Form: |
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Method: |
INTRADERMAL; INTRAMUSCULAR |
| Original Marketing Date: |
11-01-2010 |
| Category Name: |
BLA |
| Application Number: |
BLA103000 |
| Labeler: |
ALLERGAN, INC. |
| Substance Name: |
BOTULINUM TOXIN TYPE A |
| Active Numerator Strength: |
200 |
| Active Ingredient Unit: |
[USP'U]/1 |
| Pharm Classes: |
Acetylcholine Release Inhibitor [EPC],Acetylcholine Release Inhibitors [MoA] |
| DEA Schedule: |
|
