ALLOPURINOL
- Product NDC
- 61919-748
- 11-digit product format
- 619190748
- Labeler code
- 61919
- Product ID
- 61919-748_b932a9e5-7d66-0bf1-e053-2995a90a4414
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ALLOPURINOL
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- DIRECT RX
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2021-01-18
- 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
- 2022-12-31
- 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 |
|---|
| 61919-748-30 | ALLOPURINOL | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 61919-748-90 | 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 |
|---|
| 61919-748 | ALLOPURINOL TABLET [DIRECT RX] | 3 | Legacy NDC, 2 package rows | 20210119_67604124-399e-7baf-e053-2a91aa0a8ee8.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 |
|---|
| 61919-748-30 | 61919074830 | 30 TABLET in 1 BOTTLE (61919-748-30) | 30 tablet | 2021-01-18 | 0000-00-00 | No | No | Current |
| 61919-748-90 | 61919074890 | 90 TABLET in 1 BOTTLE (61919-748-90) | 90 tablet | 2021-01-18 | 0000-00-00 | No | No | Current |