NDC 70069-759 – Dexmedetomidine Hydrochloride

Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC70069-759

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine Hydrochloride
Labeler
Somerset Therapeutics, LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA218112
Marketed since
September 26, 2024
Listing expires
December 31, 2026
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Dexmedetomidine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
70069-759-044 VIAL in 1 CARTON (70069-759-04) / 10 mL in 1 VIALSep 26, 2024

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