NDC 57664-596 – Dexmedetomidine Hydrochloride

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

Human Prescription Drug

Product NDC57664-596

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine Hydrochloride
Labeler
Sun Pharmaceuticals Industries, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA202126
Marketed since
April 8, 2015
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
57664-596-5025 VIAL, SINGLE-DOSE in 1 CARTON (57664-596-50) / 2 mL in 1 VIAL, SINGLE-DOSE (57664-596-40)Apr 8, 2015

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