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
- 52536-126_f550d2ba-49ac-4a3b-95db-692b468af479
- Product NDC
- 52536-126
- Form
- INJECTION
- Composition / generic term
- dexmedetomidine hydrochloride
- Labeler
- Wilshire Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250130
- Source listing expiry
- 20261231
Source-listed ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE — 4 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 8 BOTTLE in 1 CARTON (52536-126-08) / 100 mL in 1 BOTTLE (52536-126-01) · 52536-126-08
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →