fenofibric acid
- Product NDC
- 0228-2838
- 11-digit product format
- 002282838
- Labeler code
- 0228
- Product ID
- 0228-2838_e144a22b-2b82-4826-95a6-4d2f0709817c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fenofibric acid
- Dosage form
- CAPSULE, DELAYED RELEASE
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA200920
- Marketing category
- ANDA
- Marketing start
- 2016-01-21
- Marketing end
- 2019-04-30
- Substance
- FENOFIBRIC ACID
- Active strength
- 45 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