NDC 71335-0467 – Allopurinol
Allopurinol 100 mg/1 · Tablet · Oral
Product NDC71335-0467
Product details
- Brand name
- Allopurinol
- Generic name
- Allopurinol
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA203154
- Marketed since
- April 29, 2015
- Listing expires
- December 31, 2027
- Pharmacologic class
- Xanthine Oxidase Inhibitor
Active ingredients
- Allopurinol 100 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0467-1 | 100 TABLET in 1 BOTTLE (71335-0467-1) | Apr 3, 2024 |
| 71335-0467-2 | 30 TABLET in 1 BOTTLE (71335-0467-2) | Jun 26, 2018 |
| 71335-0467-3 | 60 TABLET in 1 BOTTLE (71335-0467-3) | Aug 30, 2018 |
| 71335-0467-4 | 120 TABLET in 1 BOTTLE (71335-0467-4) | Apr 3, 2024 |
| 71335-0467-5 | 20 TABLET in 1 BOTTLE (71335-0467-5) | Apr 3, 2024 |
| 71335-0467-6 | 90 TABLET in 1 BOTTLE (71335-0467-6) | Feb 20, 2018 |
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