Allopurinol
- Product NDC
- 63629-6405
- 11-digit product format
- 636296405
- Labeler code
- 63629
- Product ID
- 63629-6405_42bb5684-e030-490a-842e-9828c95df0d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018877
- Marketing category
- NDA
- Marketing start
- 2009-04-06
- 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
- 2021-12-31
- 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 |
|---|
| 63629-6405-1 | 63629640501 | 30 TABLET in 1 BOTTLE (63629-6405-1) | 30 tablet | 2015-09-17 | 0000-00-00 | No | No | Current |