Dexmedetomidine 71288-0505-03

Package NDC

71288-0505-03

Manufacturer: Meitheal Pharmaceuticals Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: January 18, 2019
Listing Expires: December 31, 2026
Application: ANDA204843

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Active Ingredients

Ingredient	Strength
Dexmedetomidine Hydrochloride	100 ug/mL

Drug Class

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

Selected Package

71288-0505-03Selected

25 VIAL, SINGLE-DOSE in 1 CARTON (71288-505-03) / 2 mL in 1 VIAL, SINGLE-DOSE (71288-505-02)