Fenofibrate
- Product NDC
- 68788-7932
- 11-digit product format
- 687887932
- Labeler code
- 68788
- Product ID
- 68788-7932_da358160-8a43-4ce1-b0d9-dad1a141f459
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA202856
- Marketing category
- ANDA
- Marketing start
- 2021-06-15
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 145 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- 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 |
|---|
| 68788-7932 | FENOFIBRATE TABLET, FILM COATED [PREFERRED PHARMACEUTICALS INC.] | 5 | Legacy NDC | 20250511_ceedfb5d-8a04-4b4b-852f-1eac963f96a3.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7932-1 | 68788793201 | 100 TABLET, FILM COATED in 1 BOTTLE, PUMP (68788-7932-1) | 2021-06-15 | 0000-00-00 | No | No | Current |
| 68788-7932-3 | 68788793203 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7932-3) | 2021-06-15 | 0000-00-00 | No | No | Current |
| 68788-7932-6 | 68788793206 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7932-6) | 2021-06-15 | 0000-00-00 | No | No | Current |
| 68788-7932-9 | 68788793209 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7932-9) | 2021-06-15 | 0000-00-00 | No | No | Current |