United States · FDA National Drug Code directory
BOTOX
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0023-1145_9adba2d4-2c32-4986-a1b6-bcc17d5326d1
- Product NDC
- 0023-1145
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- onabotulinumtoxinA
- Labeler
- Allergan, Inc.
- Marketing category
- BLA
- Marketing start / end (source format)
- 19891215
- Source listing expiry
- 20271231
Source-listed ingredients
- BOTULINUM TOXIN TYPE A — 100 [USP'U]/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (0023-1145-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL · 0023-1145-01
- 1 VIAL in 1 CARTON (0023-1145-02) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL · 0023-1145-02
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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