Allopurinol
- Product NDC
- 70518-4412
- 11-digit product format
- 705184412
- Labeler code
- 70518
- Product ID
- 70518-4412_3b8a5bce-a7fd-e2db-e063-6394a90a8021
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA018659
- Marketing category
- ANDA
- Marketing start
- 2025-07-31
- 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 |
|---|
| 70518-4412-0 | 70518441200 | 30 TABLET in 1 BLISTER PACK (70518-4412-0) | 30 tablet | 2025-07-31 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | REMEDYREPACK INC. | 2025-08-04 | HUMAN PRESCRIPTION DRUG LABEL | 1 |