NDC 36000-262 – Dexmedetomidine Hydrochloride

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

Human Prescription Drug

Product NDC36000-262

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine hydrochloride
Labeler
Baxter Healthcare Corporation
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
ANDA · ANDA208103
Marketed since
April 16, 2026
Listing expires
December 31, 2027
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
36000-262-055 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-05) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01)Apr 16, 2026
36000-262-1010 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-10) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01)Apr 16, 2026
36000-262-2525 VIAL, SINGLE-DOSE in 1 CARTON (36000-262-25) / 2 mL in 1 VIAL, SINGLE-DOSE (36000-262-01)Apr 16, 2026

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