United States · FDA National Drug Code directory
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
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
- 43066-555_d0910ea1-c3e1-44f8-b8b5-1f39ffd43290
- Product NDC
- 43066-555
- Form
- INJECTION
- Composition / generic term
- DEXMEDETOMIDINE HYDROCHLORIDE in 0.9% sodium chloride
- Labeler
- Baxter Healthcare Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190827
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 200 ug/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 BAG in 1 CARTON (43066-555-24) / 50 mL in 1 BAG · 43066-555-24
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 →