Dexmedetomidine Hydrochloride 71225-0132-02

Package NDC

71225-0132-02

Manufacturer: Slayback Pharma Llc
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 20, 2021
Listing Expires: December 31, 2026
Application: ANDA212791

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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

71225-0132-02Selected

10 BOTTLE in 1 CARTON (71225-132-02) / 50 mL in 1 BOTTLE (71225-132-01)