Allopurinol
- Product NDC
- 68071-3605
- 11-digit product format
- 680713605
- Labeler code
- 68071
- Product ID
- 68071-3605_1b1c6812-0802-5b1c-e063-6294a90a9f9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2020-09-22
- 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 |
|---|
| 68071-3605-9 | 68071360509 | 90 TABLET in 1 BOTTLE (68071-3605-9) | 90 tablet | 2024-06-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | NuCare Pharmaceuticals,Inc. | 2024-06-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |