United States · FDA National Drug Code directory
DEXMEDETOMIDINE HYDROCHLORIDE
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
- 67457-925_e4cda7fa-dac8-4de7-abc1-d1fd622795d8
- Product NDC
- 67457-925
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXMEDETOMIDINE HYDROCHLORIDE
- Labeler
- Mylan Institutional LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201113
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 400 ug/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BOTTLE in 1 CARTON (67457-925-10) / 100 mL in 1 BOTTLE (67457-925-00) · 67457-925-10
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 →