Allopurinol
- Product NDC
- 50090-7832
- 11-digit product format
- 500907832
- Labeler code
- 50090
- Product ID
- 50090-7832_2def7003-b35b-4e0c-9bca-6a0dbd83579b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211820
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- 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 |
|---|
| 50090-7832-0 | 50090783200 | 100 TABLET in 1 BOTTLE (50090-7832-0) | 100 tablet | 2025-12-18 | No | No | Historical |
| 50090-7832-1 | 50090783201 | 500 TABLET in 1 BOTTLE (50090-7832-1) | 500 tablet | 2025-12-18 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | A-S Medication Solutions | 2025-12-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |