Allopurinol
- Product NDC
- 69967-008
- 11-digit product format
- 699670008
- Labeler code
- 69967
- Product ID
- 69967-008_41b98a30-befb-42af-b7c9-a9d5efe451e1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Arise Pharamaceuticals LLC
- Application
- ANDA204467
- Marketing category
- ANDA
- Marketing start
- 2019-12-03
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69967-008-01 | Allopurinol | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 69967-008-02 | Allopurinol | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
| 69967-008-03 | Allopurinol | 1000 in 1 BOTTLE | TABLET | 1000 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69967-008 | ALLOPURINOL TABLET [ARISE PHARAMACEUTICALS LLC] | 1 | Legacy NDC, 3 package rows | 20200316_41b98a30-befb-42af-b7c9-a9d5efe451e1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69967-008-01 | 69967000801 | 100 TABLET in 1 BOTTLE (69967-008-01) | 100 tablet | 2019-12-03 | 0000-00-00 | No | No | Current |
| 69967-008-02 | 69967000802 | 500 TABLET in 1 BOTTLE (69967-008-02) | 500 tablet | 2019-12-03 | 0000-00-00 | No | No | Current |
| 69967-008-03 | 69967000803 | 1000 TABLET in 1 BOTTLE (69967-008-03) | 1000 tablet | 2019-12-03 | 0000-00-00 | No | No | Current |