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: 68083-238_29930c5a-6908-4686-aa11-1560abca3c7f
Product NDC: 68083-238
Form: INJECTION
Composition / generic term: Dexmedetomidine Hydrochloride
Labeler: Gland Pharma Limited
Marketing category: ANDA
Marketing start / end (source format): 20200603
Source listing expiry: 20271231

Source-listed ingredients

DEXMEDETOMIDINE HYDROCHLORIDE — 4 ug/mL

These values do not establish equivalence or a dose recommendation.

Packages

20 VIAL in 1 CARTON (68083-238-20) / 50 mL in 1 VIAL · 68083-238-20

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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