Allopurinol 53489-0157
Product NDC
53489-0157- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 9, 1987
- Listing Expires
- December 31, 2027
- Application
- ANDA071450
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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(5)
100 TABLET in 1 BOTTLE, PLASTIC (53489-157-01)
50 TABLET in 1 BOTTLE, PLASTIC (53489-157-02)
500 TABLET in 1 BOTTLE, PLASTIC (53489-157-05)
30 TABLET in 1 BOTTLE, PLASTIC (53489-157-07)
1000 TABLET in 1 BOTTLE, PLASTIC (53489-157-10)