NDC 48433-039
Fenofibrate 48 mg tablet, film coated
On the label: Safecor Health, LLC. It's repackaged: Safecor Health, LLC rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-3065.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Mylan Pharmaceuticals Inc. names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 48 mg
- Approval
- ANDA ANDA202856
- On the market since
- Mar 17, 2026
- Package NDCs
48433-039-0148433-039-20- Official label
- DailyMed (National Library of Medicine), updated Mar 20, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?