NDC 51655-433
Fenofibrate 145 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged from NDC 63304-449, made by Sun Pharmaceutical Industries, Inc. (Fenofibrate). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 Northwind Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 145 mg
- Approval
- ANDA ANDA200884
- On the market since
- Sep 17, 2020
- Package NDCs
51655-433-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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