NDC 70710-2009 – Allopurinol
Allopurinol 200 mg/1 · Tablet · Oral
Product NDC70710-2009
Product details
- Brand name
- Allopurinol
- Generic name
- Allopurinol
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA210117
- Marketed since
- June 17, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Allopurinol 200 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70710-2009-0 | 1000 TABLET in 1 BOTTLE (70710-2009-0) | Jun 17, 2025 |
| 70710-2009-9 | 90 TABLET in 1 BOTTLE (70710-2009-9) | Jun 17, 2025 |
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