Allopurinol
- Product NDC
- 68788-7383
- 11-digit product format
- 687887383
- Labeler code
- 68788
- Product ID
- 68788-7383_ae87bba5-37f3-468e-8422-5f45dde52b7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- allopurinol
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA203154
- Marketing category
- ANDA
- Marketing start
- 2016-09-13
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-7383 | ALLOPURINOL TABLET [PREFERRED PHARMACEUTICALS INC.] | 9 | Legacy NDC | 20250105_62866c84-fec3-4c1b-9b8b-65c0372bc8f9.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7383-3 | 68788738303 | 30 TABLET in 1 BOTTLE (68788-7383-3) | 30 tablet | 2016-09-13 | 0000-00-00 | No | No | Current |
| 68788-7383-6 | 68788738306 | 60 TABLET in 1 BOTTLE (68788-7383-6) | 60 tablet | 2016-09-13 | 0000-00-00 | No | No | Current |
| 68788-7383-9 | 68788738309 | 90 TABLET in 1 BOTTLE (68788-7383-9) | 90 tablet | 2016-09-13 | 0000-00-00 | No | No | Current |