Allopurinol
- Product NDC
- 71610-949
- 11-digit product format
- 716100949
- Labeler code
- 71610
- Product ID
- 71610-949_3f010fe3-b62e-40dd-e063-6294a90a2f7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA214443
- Marketing category
- ANDA
- Marketing start
- 2024-05-01
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- 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 |
|---|
| 71610-949-60 | 71610094960 | 90 TABLET in 1 BOTTLE (71610-949-60) | 90 tablet | 2025-09-17 | No | No | Historical |
| 71610-949-80 | 71610094980 | 180 TABLET in 1 BOTTLE (71610-949-80) | 180 tablet | 2025-09-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Aphena Pharma Solutions - Tennessee, LLC | 2025-09-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |