Allopurinol
- Product NDC
- 72162-1149
- 11-digit product format
- 721621149
- Labeler code
- 72162
- Product ID
- 72162-1149_90912dd4-5abf-4fd3-8fc1-3afd057b743f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075798
- Marketing category
- ANDA
- Marketing start
- 2003-06-27
- 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 |
|---|
| 72162-1149-0 | 72162114900 | 1000 TABLET in 1 BOTTLE (72162-1149-0) | 1000 tablet | 2003-06-27 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Bryant Ranch Prepack | 2024-04-08 | HUMAN PRESCRIPTION DRUG LABEL | 103 |