NDC 0115-5511-01
FENOFIBRATE 54 mg/1
FENOFIBRATE · TABLET
FENOFIBRATE is a tablet containing fenofibrate at a strength of 54 mg/1. Manufactured by Amneal Pharmaceuticals of New York LLC.
Key Facts
- Brand Name
- FENOFIBRATE
- Generic Name
- FENOFIBRATE
- NDC Code (Package)
0115-5511-01- NDC Code (Product)
0115-5511- Manufacturer
- Amneal Pharmaceuticals of New York LLC
- Strength
- 54 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076509
- Drug Class
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- Marketing Start
- 02/01/2010
Recall History
No Recall HistoryView Full Drug Page
FENOFIBRATE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.