FDA NDC

BOTOX

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
0023-1145
Proprietary name
BOTOX
Nonproprietary name
onabotulinumtoxinA
Labeler
Allergan, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Strength
100 [USP'U]/1

Run it in Rivvi

Which 2027 plans near you dropped or restricted onabotulinumtoxinA?

Tier changes and new prior auth, step therapy or quantity limits, plan by plan, from the CMS Part D files.

Free to start. Opens Rivvi, the AI workspace for healthcare teams.

Try it on your own data today.

Free to start. Most teams are using it the same day.