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
- 43598-976_5785a11f-7784-4ae0-8029-f50b782eaf4a
- Product NDC
- 43598-976
- Form
- INJECTION, SOLUTION
- Composition / generic term
- DEXMEDETOMIDINE HYDROCHLORIDE
- Labeler
- Dr.Reddy's Laboratories Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200817
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 4 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL in 1 CARTON (43598-976-58) / 50 mL in 1 VIAL (43598-976-11) · 43598-976-58
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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