Fenofibrate
- Product NDC
- 68788-7662
- 11-digit product format
- 687887662
- Labeler code
- 68788
- Product ID
- 68788-7662_79333850-4d27-457c-8057-016a0048ad19
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA209660
- Marketing category
- ANDA
- Marketing start
- 2020-02-28
- 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
- 2022-12-31
- 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 |
|---|
| 68788-7662-1 | 68788766201 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-7662-1) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7662-3 | 68788766203 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7662-3) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7662-6 | 68788766206 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7662-6) | 2020-02-28 | 0000-00-00 | No | No | Current |
| 68788-7662-9 | 68788766209 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7662-9) | 2020-02-28 | 0000-00-00 | No | No | Current |