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
- 55150-209_a1eab62d-fcef-4b83-9266-3c5f7a05927b
- Product NDC
- 55150-209
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dexmedetomidine
- Labeler
- Eugia US LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160317
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 100 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL in 1 CARTON (55150-209-02) / 2 mL in 1 VIAL · 55150-209-02
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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