Fenofibrate
- Product NDC
- 68682-495
- 11-digit product format
- 686820495
- Labeler code
- 68682
- Product ID
- 68682-495_e580947c-c955-4810-8182-05d47b35bfeb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA022118
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2021-03-16
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 120 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68682-495-90 | 68682049590 | 90 TABLET in 1 BOTTLE (68682-495-90) | 90 tablet | 2021-03-16 | 0000-00-00 | No | No | Current |