United States · FDA National Drug Code directory
Dexmedetomidine Hydrochloride in Sodium Chloride
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
- 68094-147_721350a6-f9ae-4c06-b8b5-41169d7cd43e
- Product NDC
- 68094-147
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Dexmedetomidine Hydrochloride
- Labeler
- Precision Dose, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201123
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 4 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 BOTTLE in 1 CARTON (68094-147-20) / 50 mL in 1 BOTTLE (68094-147-01) · 68094-147-20
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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