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
- 70121-1711_06a08ff5-3a87-427a-9ecd-3a4300953037
- Product NDC
- 70121-1711
- Form
- INJECTION
- Composition / generic term
- Dexmedetomidine Hydrochloride in Sodium Chloride
- Labeler
- Amneal Pharmaceuticals LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230519
- Source listing expiry
- 20271231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 4 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 15 POUCH in 1 CARTON (70121-1711-2) / 1 BAG in 1 POUCH / 50 mL in 1 BAG · 70121-1711-2
- 24 POUCH in 1 CARTON (70121-1711-9) / 1 BAG in 1 POUCH / 50 mL in 1 BAG · 70121-1711-9
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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