Allopurinol
- Product NDC
- 50090-3760
- 11-digit product format
- 500903760
- Labeler code
- 50090
- Product ID
- 50090-3760_e1b1bafa-6030-4de5-9590-0c6eef031168
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA071450
- Marketing category
- ANDA
- Marketing start
- 1987-01-09
- 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
- 2020-12-31
- 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 |
|---|
| 50090-3760-3 | Allopurinol | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | | 3 |
| 50090-3760-4 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3760 | ALLOPURINOL TABLET [A-S MEDICATION SOLUTIONS] | 3 | Legacy NDC, 2 package rows | 20190430_bfd3bd12-ebe7-486c-8338-824b05fff1b1.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 |
|---|
| 50090-3760-3 | 50090376003 | 30 TABLET in 1 BOTTLE, PLASTIC (50090-3760-3) | 30 tablet | 2014-11-28 | 0000-00-00 | No | No | Current |
| 50090-3760-4 | 50090376004 | 90 TABLET in 1 BOTTLE (50090-3760-4) | 90 tablet | 2018-11-01 | 0000-00-00 | No | No | Current |