NDC 69367-254
Fenofibrate 160 mg tablet, film coated
On the label: Westminster Pharmaceuticals, LLC.
Where it's 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
- Apr 23, 2020
- Package NDCs
69367-254-0569367-254-09- Official label
- DailyMed (National Library of Medicine), updated Sep 29, 2026
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