United States · FDA National Drug Code directory
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% 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
- 0781-3494_5a0d944c-af38-a3fd-e063-6294a90aed62
- Product NDC
- 0781-3494
- Form
- INJECTION
- Composition / generic term
- DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
- Labeler
- Sandoz Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200612
- 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 (0781-3494-95) / 50 mL in 1 BOTTLE · 0781-3494-95
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 →