NDC 68071-2686
Fenofibrate 145 mg tablet, film coated
On the label: NuCare Pharmaceuticals.Inc.. It's repackaged: NuCare Pharmaceuticals.Inc. rebottles it from Mylan Pharmaceuticals Inc.'s NDC 0378-3066.
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.
Repackaging site
- NuCare Pharmaceuticals,Inc., Orange, CA, United States · relabels it
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, film coated
- Strength
- 145 mg
- Approval
- ANDA ANDA202856
- On the market since
- May 14, 2013
- Package NDCs
68071-2686-9- Official label
- DailyMed (National Library of Medicine), updated May 4, 2022
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