NDC 70518-4672
Fenofibrate 145 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Solco Healthcare U.S., LLC's NDC 43547-431.
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 Solco Healthcare U.S., LLC names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet, oral
- Strength
- 145 mg
- Approval
- ANDA ANDA211080
- On the market since
- May 27, 2026
- Package NDCs
70518-4672-070518-4672-1- Official label
- DailyMed (National Library of Medicine), updated Jun 1, 2026
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