NDC 60219-5522-5
FENOFIBRATE 160 mg/1
FENOFIBRATE · TABLET
FENOFIBRATE is a tablet containing fenofibrate at a strength of 160 mg/1. Manufactured by Amneal Pharmaceuticals NY LLC.
Key Facts
- Brand Name
- FENOFIBRATE
- Generic Name
- FENOFIBRATE
- NDC Code (Package)
60219-5522-5- NDC Code (Product)
60219-5522- Manufacturer
- Amneal Pharmaceuticals NY LLC
- Strength
- 160 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA076509
- Drug Class
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- Marketing Start
- 06/22/2022
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.