Allopurinol 55111-0729
Product NDC
55111-0729- Manufacturer
- Dr. Reddy's Laboratories Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 1, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA071586
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Allopurinol | 100 mg/1 |
Drug Class
Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]
Packaging Options(2)
100 TABLET in 1 BOTTLE (55111-729-01)
1000 TABLET in 1 BOTTLE (55111-729-10)