Allopurinol
- Product NDC
- 70771-1907
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA210117
- Marketing category
- ANDA
- Substance
- ALLOPURINOL
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70771-1907-0 | 1000 TABLET in 1 BOTTLE (70771-1907-0) | 2025-06-17 | | No | Historical |
| 70771-1907-9 | 90 TABLET in 1 BOTTLE (70771-1907-9) | 2025-06-17 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allopurinol | Zydus Lifesciences Limited | 2025-06-18 | HUMAN PRESCRIPTION DRUG LABEL | 6 |