Allopurinol
- Product NDC
- 10544-911
- 11-digit product format
- 105440911
- Labeler code
- 10544
- Product ID
- 10544-911_147e8c8b-4884-1e43-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Blenheim Pharmacal, Inc.
- Application
- ANDA071587
- Marketing category
- ANDA
- Marketing start
- 2015-04-21
- 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
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 10544-911-30 | Allopurinol | 20 in 1 BOTTLE | TABLET | 20 | | 1 |
| 10544-911-90 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10544-911 | ALLOPURINOL TABLET [BLENHEIM PHARMACAL, INC.] | 1 | Legacy NDC, 2 package rows | 20150425_147e8c8b-4883-1e43-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 10544-911-30 | 10544091130 | 20 in 1 BOTTLE | Historical |
| 10544-911-90 | 10544091190 | 90 in 1 BOTTLE | Historical |