Allopurinol
- Product NDC
- 67046-0681
- 11-digit product format
- 670460681
- Labeler code
- 67046
- Product ID
- 67046-0681_6a275cd1-052a-1312-e053-2991aa0a9ee0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Coupler LLC
- Application
- ANDA018659
- Marketing category
- ANDA
- Marketing start
- 2018-02-23
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 67046-0681-3 | 67046068103 | 30 TABLET in 1 BLISTER PACK (67046-0681-3) | 30 tablet | 2018-02-23 | No | No | Historical |