NDC 71335-9676 – Allopurinol
Allopurinol 300 mg/1 · Tablet · Oral
Product NDC71335-9676
Product details
- Brand name
- Allopurinol
- Generic name
- Allopurinol
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA018659
- Marketed since
- October 24, 1986
- Listing expires
- December 31, 2027
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Allopurinol 300 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-9676-1 | 30 TABLET in 1 BOTTLE (71335-9676-1) | Jul 8, 2024 |
| 71335-9676-2 | 60 TABLET in 1 BOTTLE (71335-9676-2) | Apr 13, 2026 |
| 71335-9676-3 | 100 TABLET in 1 BOTTLE (71335-9676-3) | Mar 13, 2024 |
| 71335-9676-4 | 90 TABLET in 1 BOTTLE (71335-9676-4) | Apr 19, 2023 |
| 71335-9676-5 | 20 TABLET in 1 BOTTLE (71335-9676-5) | Apr 13, 2026 |
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