Allopurinol 16571-0884
Product NDC
16571-0884- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 21, 2023
- Listing Expires
- December 31, 2027
- Application
- NDA016084
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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(4)
100 TABLET in 1 BOTTLE (16571-884-01)
90 TABLET in 1 BOTTLE (16571-884-09)
1000 TABLET in 1 BOTTLE (16571-884-10)
500 TABLET in 1 BOTTLE (16571-884-50)