Fenofibrate
- Product NDC
- 68788-7340
- 11-digit product format
- 687887340
- Labeler code
- 68788
- Product ID
- 68788-7340_35ae7165-608a-4c26-bee8-96f85515d3de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076433
- Marketing category
- ANDA
- Marketing start
- 2019-03-12
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 160 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7340-1 | 68788734001 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7340-1) | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7340-3 | 68788734003 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7340-3) | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7340-6 | 68788734006 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7340-6) | 2019-03-12 | 0000-00-00 | No | No | Current |
| 68788-7340-9 | 68788734009 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7340-9) | 2019-03-12 | 0000-00-00 | No | No | Current |