Allopurinol
- Product NDC
- 68788-7542
- 11-digit product format
- 687887542
- Labeler code
- 68788
- Product ID
- 68788-7542_e5d27cfb-5f0a-4237-b937-b6db6f9f9028
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA210117
- Marketing category
- ANDA
- Marketing start
- 2018-02-08
- 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
- 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 |
|---|
| 68788-7542-1 | Allopurinol | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
| 68788-7542-3 | Allopurinol | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 68788-7542-9 | Allopurinol | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7542 | ALLOPURINOL TABLET [PREFERRED PHARMACEUTICALS, INC.] | 2 | Legacy NDC, 3 package rows | 20210224_0c4431bc-e514-4e89-9495-025a24f399d0.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 |
|---|
| 68788-7542-1 | 68788754201 | 100 TABLET in 1 BOTTLE (68788-7542-1) | 100 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7542-3 | 68788754203 | 30 TABLET in 1 BOTTLE (68788-7542-3) | 30 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |
| 68788-7542-9 | 68788754209 | 90 TABLET in 1 BOTTLE (68788-7542-9) | 90 tablet | 2019-12-27 | 0000-00-00 | No | No | Current |