United States · FDA National Drug Code directory
Dexmedetomidine
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
- 83634-600_f036291f-40af-44b9-8a7f-d4475788ea63
- Product NDC
- 83634-600
- Form
- INJECTION, SOLUTION, CONCENTRATE
- Composition / generic term
- dexmedetomidine
- Labeler
- Avenacy Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240315 / 20270401
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 100 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (83634-600-02) / 2 mL in 1 VIAL (83634-600-41) · 83634-600-02
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →