Allopurinol
- Product NDC
- 71335-2347
- 11-digit product format
- 713352347
- Labeler code
- 71335
- Product ID
- 71335-2347_bf1291e8-9e9a-47c8-a578-5f3b6647a904
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2020-09-22
- Marketing end
- 2029-10-31
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- 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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-2347-1 | 71335234701 | 100 TABLET in 1 BOTTLE (71335-2347-1) | 100 tablet | 2024-05-22 | 2029-10-31 | No | No | Historical |
| 71335-2347-2 | 71335234702 | 30 TABLET in 1 BOTTLE (71335-2347-2) | 30 tablet | 2024-03-14 | 2029-10-31 | No | No | Historical |
| 71335-2347-3 | 71335234703 | 60 TABLET in 1 BOTTLE (71335-2347-3) | 60 tablet | 2024-05-22 | 2029-10-31 | No | No | Historical |
| 71335-2347-4 | 71335234704 | 120 TABLET in 1 BOTTLE (71335-2347-4) | 120 tablet | 2024-05-22 | 2029-10-31 | No | No | Historical |
| 71335-2347-5 | 71335234705 | 20 TABLET in 1 BOTTLE (71335-2347-5) | 20 tablet | 2024-05-22 | 2029-10-31 | No | No | Historical |
| 71335-2347-6 | 71335234706 | 90 TABLET in 1 BOTTLE (71335-2347-6) | 90 tablet | 2024-03-07 | 2029-10-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Bryant Ranch Prepack | 2026-05-13 | HUMAN PRESCRIPTION DRUG LABEL | 102 |