Allopurinol 65219-0380
Product NDC
65219-0380- 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]
Packaging Options(1)
1 VIAL, GLASS in 1 CARTON (65219-380-30) / 25 mL in 1 VIAL, GLASS