Allopurinol
- Product NDC
- 71335-2332
- 11-digit product format
- 713352332
- Labeler code
- 71335
- Product ID
- 71335-2332_57b560f3-12bf-4568-8539-0b84e113ab49
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211820
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 71335-2332-1 | 71335233201 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2332-1) | 30 tablet | 2024-04-03 | No | No | Historical |
| 71335-2332-2 | 71335233202 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2332-2) | 60 tablet | 2024-04-03 | No | No | Historical |
| 71335-2332-3 | 71335233203 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2332-3) | 100 tablet | 2024-03-13 | No | No | Historical |
| 71335-2332-4 | 71335233204 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2332-4) | 90 tablet | 2024-04-03 | No | No | Historical |
| 71335-2332-5 | 71335233205 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-2332-5) | 20 tablet | 2024-04-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Bryant Ranch Prepack | 2026-05-15 | HUMAN PRESCRIPTION DRUG LABEL | 102 |