Dexmedetomidine Hydrochloride 70121-1389-07

Package NDC

70121-1389-07

Manufacturer: Amneal Pharmaceuticals Llc
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 20, 2020
Listing Expires: December 31, 2026
Application: ANDA207551

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Active Ingredients

Ingredient	Strength
Dexmedetomidine Hydrochloride	4 ug/mL

Drug Class

Adrenergic alpha2-Agonists [MoA]Central alpha-2 Adrenergic Agonist [EPC]General Anesthesia [PE]

Selected Package

70121-1389-07Selected

10 BOTTLE, GLASS in 1 CARTON (70121-1389-7) / 100 mL in 1 BOTTLE, GLASS (70121-1389-1)