Allopurinol
- Product NDC
- 67046-022
- 11-digit product format
- 670460022
- Labeler code
- 67046
- Product ID
- 67046-022_57fa94ed-b29f-456a-e053-2a91aa0af484
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacy Services-PA
- 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 |
|---|
| 67046-022-30 | Allopurinol | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67046-022 | ALLOPURINOL TABLET [CONTRACT PHARMACY SERVICES-PA] | 1 | Legacy NDC, 1 package rows | 20170831_57fa94ed-b29e-456a-e053-2a91aa0af484.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 |
|---|
| 67046-022-30 | 67046002230 | 30 TABLET in 1 BLISTER PACK (67046-022-30) | 30 tablet | 2017-08-30 | 0000-00-00 | No | No | Current |