Allopurinol
- Product NDC
- 71610-676
- 11-digit product format
- 716100676
- Labeler code
- 71610
- Product ID
- 71610-676_e28187c8-a987-4806-8652-c28f514db907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2020-09-22
- 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 |
|---|
| 71610-676-53 | 71610067653 | 60 TABLET in 1 BOTTLE (71610-676-53) | 60 tablet | 2022-11-11 | No | No | Historical |
| 71610-676-60 | 71610067660 | 90 TABLET in 1 BOTTLE (71610-676-60) | 90 tablet | 2022-11-11 | No | No | Historical |
| 71610-676-80 | 71610067680 | 180 TABLET in 1 BOTTLE (71610-676-80) | 180 tablet | 2022-11-11 | No | No | Historical |