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
- 72572-127_8906e391-411f-456b-8263-17e0e05bbb35
- Product NDC
- 72572-127
- Form
- INJECTION
- Composition / generic term
- dexmedetomidine hydrochloride
- Labeler
- CIVICA, INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210823
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 4 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BOTTLE in 1 CARTON (72572-127-10) / 50 mL in 1 BOTTLE (72572-127-01) · 72572-127-10
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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