Fenofibrate
- Product NDC
- 0615-8165
- 11-digit product format
- 006158165
- Labeler code
- 0615
- Product ID
- 0615-8165_ef92e137-29b2-4e42-8f6b-a9abf7f8dea4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fenofibrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA204019
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- Marketing end
- 2020-11-30
- Substance
- FENOFIBRATE
- Active strength
- 160 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