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
- 71872-7323_12ef0602-bf08-6ddd-e063-6294a90a23c3
- Product NDC
- 71872-7323
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dexmedetomidine
- Labeler
- Medical Purchasing Solutions, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210119
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 200 ug/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 BAG (71872-7323-1) / 2 mL in 1 VIAL, GLASS · 71872-7323-1
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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