Allopurinol
- Product NDC
- 63629-8021
- 11-digit product format
- 636298021
- Labeler code
- 63629
- Product ID
- 63629-8021_a2d38716-3790-468c-abe8-22f79690f072
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2015-04-29
- Marketing end
- 0000-00-00
- Substance
- ALLOPURINOL
- Active strength
- 300 mg/1
- Pharmacologic classes
- Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 63629-8021-1 | 63629802101 | 90 TABLET in 1 BOTTLE (63629-8021-1) | 90 tablet | 2019-07-18 | 0000-00-00 | No | No | Current |