NDC 70121-1388 – Dexmedetomidine Hydrochloride

Dexmedetomidine Hydrochloride 4 ug/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC70121-1388

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA207551
Marketed since
May 20, 2020
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 (1)

Package NDCDescriptionSince
70121-1388-820 BOTTLE, GLASS in 1 CARTON (70121-1388-8) / 50 mL in 1 BOTTLE, GLASS (70121-1388-1)May 20, 2020

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