Allopurinol 65219-0380-30

Package NDC

65219-0380-30

Manufacturer: Fresenius Kabi Usa, Llc
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: March 14, 2022
Listing Expires: December 31, 2026
Application: ANDA212363

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Active Ingredients

Ingredient	Strength
Allopurinol Sodium	500 mg/25mL

Drug Class

Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]

Selected Package

65219-0380-30Selected

1 VIAL, GLASS in 1 CARTON (65219-380-30) / 25 mL in 1 VIAL, GLASS