FENOFIBRATE
- Product NDC
- 0179-0103
- 11-digit product format
- 001790103
- Labeler code
- 0179
- Product ID
- 0179-0103_7baea303-1390-5a69-e053-2991aa0a5f54
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FENOFIBRATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- KAISER FOUNDATION HOSPITALS
- Application
- ANDA076509
- Marketing category
- ANDA
- Marketing start
- 2011-08-03
- Marketing end
- 2020-06-30
- Substance
- FENOFIBRATE
- Active strength
- 54 mg/1
- Pharmacologic classes
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record