Allopurinol 53489-0156
Product NDC
53489-0156- 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
Need to source Allopurinol? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Allopurinol | 100 mg/1 |
Drug Class
Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitor [EPC]Xanthine Oxidase Inhibitors [MoA]
Packaging Options(4)
100 TABLET in 1 BOTTLE, PLASTIC (53489-156-01)
50 TABLET in 1 BOTTLE, PLASTIC (53489-156-02)
500 TABLET in 1 BOTTLE, PLASTIC (53489-156-05)
1000 TABLET in 1 BOTTLE, PLASTIC (53489-156-10)