NDC 42291-427
Fenofibrate 160 mg tablet, film coated
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Westminster Pharmaceuticals, LLC's NDC 69367-254.
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 Westminster Pharmaceuticals, LLC names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 160 mg
- Approval
- ANDA ANDA207803
- On the market since
- Mar 8, 2023
- Package NDCs
42291-427-5042291-427-90- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?