Allopurinol 70771-1907
Product NDC
70771-1907- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 17, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA210117
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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(2)
1000 TABLET in 1 BOTTLE (70771-1907-0)
90 TABLET in 1 BOTTLE (70771-1907-9)