fenofibrate
- Product NDC
- 71335-0578
- 11-digit product format
- 713350578
- Labeler code
- 71335
- Product ID
- 71335-0578_c329ae96-c1b2-44c8-aea9-9fa5b9877649
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA090715
- Marketing category
- ANDA
- Marketing start
- 2014-08-13
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 48 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0578-1 | 71335057801 | 30 TABLET in 1 BOTTLE (71335-0578-1) | 30 tablet | 2014-08-13 | 0000-00-00 | No | No | Current |
| 71335-0578-2 | 71335057802 | 90 TABLET in 1 BOTTLE (71335-0578-2) | 90 tablet | 2014-08-13 | 0000-00-00 | No | No | Current |
| 71335-0578-3 | 71335057803 | 28 TABLET in 1 BOTTLE (71335-0578-3) | 28 tablet | 2018-04-30 | 0000-00-00 | No | No | Current |