BOTOX 100 [USP'U]/1
onabotulinumtoxinA · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · Allergan, Inc.
No Recall History
Plain English
BOTOX is a injection, powder, lyophilized, for solution containing onabotulinumtoxina at 100 [USP'U]/1, taken intradermal. Manufactured by Allergan, Inc..
Key Facts
- Brand Name
- BOTOX
- Generic Name
- onabotulinumtoxinA
- 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 HistoryFrequently Asked Questions
What is BOTOX used for?
BOTOX contains onabotulinumtoxinA. It is a injection, powder, lyophilized, for solution taken intradermal. Consult your doctor for specific uses.
Is BOTOX a controlled substance?
BOTOX is not classified as a controlled substance by the DEA.
What is the generic name for BOTOX?
The generic name for BOTOX is onabotulinumtoxinA. There are 2 other brand versions of onabotulinumtoxinA.
What is the NDC code for BOTOX 100 [USP'U]/1?
The NDC (National Drug Code) for BOTOX 100 [USP'U]/1 is 0023-1145, listed by Allergan, Inc..