Fenofibrate
- Product NDC
- 68788-6330
- 11-digit product format
- 687886330
- Labeler code
- 68788
- Product ID
- 68788-6330_e140dece-8229-48a6-a828-664c082c7850
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2016-10-17
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record