Allopurinol
- Product NDC
- 63629-6508
- 11-digit product format
- 636296508
- Labeler code
- 63629
- Product ID
- 63629-6508_7d616c50-d885-42c3-a244-617fe65c0830
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018832
- Marketing category
- NDA
- Marketing start
- 2009-04-06
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-6508-1 | 63629650801 | 30 TABLET in 1 BOTTLE (63629-6508-1) | 30 tablet | 2015-07-27 | 0000-00-00 | No | No | Current |
| 63629-6508-2 | 63629650802 | 60 TABLET in 1 BOTTLE (63629-6508-2) | 60 tablet | 2015-07-27 | 0000-00-00 | No | No | Current |
| 63629-6508-3 | 63629650803 | 90 TABLET in 1 BOTTLE (63629-6508-3) | 90 tablet | 2015-07-27 | 0000-00-00 | No | No | Current |
| 63629-6508-4 | 63629650804 | 180 TABLET in 1 BOTTLE (63629-6508-4) | 180 tablet | 2015-07-27 | 0000-00-00 | No | No | Current |