Allopurinol
- Product NDC
- 53217-187
- 11-digit product format
- 532170187
- Labeler code
- 53217
- Product ID
- 53217-187_2ca799ba-56af-4fa6-ac9c-44f736ef1a02
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- 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
- 2019-12-31
- 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 |
|---|
| 53217-187-00 | Allopurinol | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 53217-187-30 | Allopurinol | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
| 53217-187-60 | Allopurinol | 60 in 1 BOTTLE | TABLET | 60 | | 1 |
| 53217-187-90 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-187 | ALLOPURINOL TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 4 package rows | 20170225_c9a01871-bbf8-4b31-9b9b-9fa8c0997b29.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-187-00 | 53217018700 | 100 in 1 BOTTLE | Historical |
| 53217-187-30 | 53217018730 | 30 in 1 BOTTLE | Historical |
| 53217-187-60 | 53217018760 | 60 in 1 BOTTLE | Historical |
| 53217-187-90 | 53217018790 | 90 in 1 BOTTLE | Historical |