NDC 42385-936-11
FENOFIBRATE 160 mg/1
FENOFIBRATE · TABLET, FILM COATED
FENOFIBRATE is a tablet, film coated containing fenofibrate at a strength of 160 mg/1. Manufactured by Laurus Labs Limited.
Key Facts
- Brand Name
- FENOFIBRATE
- Generic Name
- FENOFIBRATE
- NDC Code (Package)
42385-936-11- NDC Code (Product)
42385-936- Manufacturer
- Laurus Labs Limited
- Strength
- 160 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA210606
- Drug Class
- Peroxisome Proliferator Receptor alpha Agonist [EPC]
- Marketing Start
- 01/13/2020
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.