NDC 70934-224
Fenofibrate 145 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated
- Strength
- 145 mg
- Approval
- ANDA ANDA200884
- On the market since
- Jan 8, 2019
- Package NDCs
70934-224-30- Official label
- DailyMed (National Library of Medicine), updated Jan 13, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?