NDC 0023-1145-01
BOTOX 100 [USP'U]/1
onabotulinumtoxinA · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
BOTOX is a injection, powder, lyophilized, for solution containing onabotulinumtoxina at a strength of 100 [USP'U]/1. Manufactured by Allergan, Inc..
Key Facts
- Brand Name
- BOTOX
- Generic Name
- onabotulinumtoxinA
- NDC Code (Package)
0023-1145-01- NDC Code (Product)
0023-1145- Manufacturer
- Allergan, Inc.
- Strength
- 100 [USP'U]/1
- Dosage Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRADERMAL, INTRAMUSCULAR
- Marketing Status
- Application #
- BLA103000
- Drug Class
- Acetylcholine Release Inhibitor [EPC]; Neuromuscular Blocker [EPC]
- Marketing Start
- 12/15/1989
Recall History
No Recall HistoryView Full Drug Page
BOTOX — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.