fenofibrate
- Product NDC
- 68071-4265
- 11-digit product format
- 680714265
- Labeler code
- 68071
- Product ID
- 68071-4265_64434256-5fce-3a23-e053-2991aa0afee2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record