ALLOPURINOL
- Product NDC
- 61919-748
- 11-digit product format
- 619190748
- Labeler code
- 61919
- Product ID
- 61919-748_b932a9e5-7d66-0bf1-e053-2995a90a4414
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2021-01-18
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 100 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 61919-748-30 | 61919074830 | 30 TABLET in 1 BOTTLE (61919-748-30) | 30 tablet | 2021-01-18 | 0000-00-00 | No | No | Current |
| 61919-748-90 | 61919074890 | 90 TABLET in 1 BOTTLE (61919-748-90) | 90 tablet | 2021-01-18 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ALLOPURINOL | DIRECT RX | 2021-01-18 | HUMAN PRESCRIPTION DRUG LABEL | 3 |