Fenofibrate
- Product NDC
- 68071-2115
- 11-digit product format
- 680712115
- Labeler code
- 68071
- Product ID
- 68071-2115_48209b78-13b8-09b6-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- NDA021656
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-02-09
- Marketing end
- 0000-00-00
- Substance
- FENOFIBRATE
- Active strength
- 145 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