Fenofibrate
- Product NDC
- 68071-4659
- 11-digit product format
- 680714659
- Labeler code
- 68071
- Product ID
- 68071-4659_7cd65ff7-d032-dd5f-e053-2a91aa0afb56
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA200884
- Marketing category
- ANDA
- Marketing start
- 2018-06-28
- 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