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
- 0338-9557_594e9faa-bc32-42e0-9c0a-8fa9460b1e24
- Product NDC
- 0338-9557
- Form
- INJECTION
- Composition / generic term
- DEXMEDETOMIDINE HYDROCHLORIDE
- Labeler
- Baxter Healthcare Company
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180821
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 400 ug/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BAG in 1 CARTON (0338-9557-12) / 100 mL in 1 BAG · 0338-9557-12
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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