Allopurinol
- Product NDC
- 72189-647
- 11-digit product format
- 721890647
- Labeler code
- 72189
- Product ID
- 72189-647_426262e6-821a-c825-e063-6294a90a21a9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA217748
- Marketing category
- ANDA
- Marketing start
- 2025-10-30
- Substance
- ALLOPURINOL
- Active strength
- 300 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 |
|---|
| 72189-647-90 | 72189064790 | 90 TABLET in 1 BOTTLE (72189-647-90) | 90 tablet | 2025-10-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Direct_Rx | 2025-10-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |