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
- 57664-596_1086cd9a-8975-4c42-a120-f8b70c9a7bdb
- Product NDC
- 57664-596
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXMEDETOMIDINE HYDROCHLORIDE
- Labeler
- Sun Pharmaceuticals Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150408
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 100 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-DOSE in 1 CARTON (57664-596-50) / 2 mL in 1 VIAL, SINGLE-DOSE (57664-596-40) · 57664-596-50
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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