Allopurinol
- Product NDC
- 43063-976
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA071450
- Marketing category
- ANDA
- Substance
- ALLOPURINOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 43063-976-30 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-976-30) | 20190820 | | No | Historical |
| 43063-976-90 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-976-90) | 20190429 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 211e47c6-85b9-43e8-9e07-6cc4b8f708a0 | These highlights do not include all the information needed to use ALLOPURINOL TABLETS safely and effectively. See full prescribing information for ALLOPURINOL TABLETS. ALLOPURINOL tablets, for oral use Initial U.S. Approval: 1966 | PD-Rx Pharmaceuticals, Inc. | 2025-10-17 | HUMAN PRESCRIPTION DRUG LABEL | 16 |
| 211e47c6-85b9-43e8-9e07-6cc4b8f708a0 | These highlights do not include all the information needed to use ALLOPURINOL TABLETS safely and effectively. See full prescribing information for ALLOPURINOL TABLETS. ALLOPURINOL tablets, for oral use Initial U.S. Approval: 1966 | PD-Rx Pharmaceuticals, Inc. | 2024-07-12 | HUMAN PRESCRIPTION DRUG LABEL | 15 |