Drugplain

BOTOX 200 [USP'U]/1

onabotulinumtoxinA · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · Allergan, Inc.

No Recall History
Plain English

Botox is an injectable medication that works by blocking the release of acetylcholine, a chemical messenger in your nerves, to reduce muscle contractions. It is prescribed to treat conditions like wrinkles, muscle spasms, migraines, and certain eye movement disorders.

Key Facts

Brand Name
BOTOX
Generic Name
onabotulinumtoxinA
NDC Code (Product)
0023-3921
Manufacturer
Allergan, Inc.
Strength
200 [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
01/11/2010

Recall History

No Recall History

Frequently Asked Questions

What is BOTOX used for?

Botox is an injectable medication that works by blocking the release of acetylcholine, a chemical messenger in your nerves, to reduce muscle contractions. It is prescribed to treat conditions like wrinkles, muscle spasms, migraines, and certain eye movement disorders.

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 200 [USP'U]/1?

The NDC (National Drug Code) for BOTOX 200 [USP'U]/1 is 0023-3921, listed by Allergan, Inc..

Product NDC

0023-3921

Package NDC

0023-3921-02

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)