Allopurinol 71921-0241
Product NDC
71921-0241- Manufacturer
- Florida Pharmaceutical Products, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 22, 2025
- Listing Expires
- December 31, 2027
- Application
- ANDA204467
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Allopurinol | 200 mg/1 |
Drug Class
Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]
Packaging Options(1)
90 TABLET in 1 BOTTLE (71921-241-09)