BOTOX Cosmetic 50 [USP'U]/1
onabotulinumtoxinA · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · Allergan, Inc.
No Recall History
Plain English
BOTOX Cosmetic is a injection, powder, lyophilized, for solution containing onabotulinumtoxina at 50 [USP'U]/1, taken intramuscular. Manufactured by Allergan, Inc..
Key Facts
- Brand Name
- BOTOX Cosmetic
- Generic Name
- onabotulinumtoxinA
- NDC Code (Product)
0023-3919- Manufacturer
- Allergan, Inc.
- Strength
- 50 [USP'U]/1
- Dosage Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR
- Marketing Status
- Application #
- BLA103000
- Drug Class
- Acetylcholine Release Inhibitor [EPC]; Neuromuscular Blocker [EPC]
- Marketing Start
- 07/15/2008
Recall History
No Recall HistoryFrequently Asked Questions
What is BOTOX Cosmetic used for?
BOTOX Cosmetic contains onabotulinumtoxinA. It is a injection, powder, lyophilized, for solution taken intramuscular. Consult your doctor for specific uses.
Is BOTOX Cosmetic a controlled substance?
BOTOX Cosmetic is not classified as a controlled substance by the DEA.
What is the generic name for BOTOX Cosmetic?
The generic name for BOTOX Cosmetic is onabotulinumtoxinA. There are 3 other brand versions of onabotulinumtoxinA.
What is the NDC code for BOTOX Cosmetic 50 [USP'U]/1?
The NDC (National Drug Code) for BOTOX Cosmetic 50 [USP'U]/1 is 0023-3919, listed by Allergan, Inc..