Allopurinol 68071-3672
Product NDC
68071-3672- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA214443
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Allopurinol | 300 mg/1 |
Drug Class
Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]
Packaging Options(1)
90 TABLET in 1 BOTTLE (68071-3672-9)