Allopurinol
- Product NDC
- 70710-2009
- 11-digit product format
- 707102009
- Labeler code
- 70710
- Product ID
- 70710-2009_95c7021b-a1a5-4a7f-aacf-275a64fe8b58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Application
- ANDA210117
- Marketing category
- ANDA
- Marketing start
- 2025-06-17
- Substance
- ALLOPURINOL
- Active strength
- 200 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 63CZ7GJN5I | ALLOPURINOL | 315-30-0 | ALLOPURINOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70710-2009-0 | 70710200900 | 1000 TABLET in 1 BOTTLE (70710-2009-0) | 1000 tablet | 2025-06-17 | No | No | Historical |
| 70710-2009-9 | 70710200909 | 90 TABLET in 1 BOTTLE (70710-2009-9) | 90 tablet | 2025-06-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Zydus Pharmaceuticals (USA) Inc. | Zydus Lifesciences Limited | 2025-04-07 | HUMAN PRESCRIPTION DRUG LABEL | 6 |