Allopurinol
- Product NDC
- 68071-3803
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA214443
- Marketing category
- ANDA
- Substance
- ALLOPURINOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3803-3 | 30 TABLET in 1 BOTTLE (68071-3803-3) | 2025-02-27 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | NuCare Pharmaceuticals, Inc. | 2025-02-27 | HUMAN PRESCRIPTION DRUG LABEL | 1 |