NDC 72189-026
Fenofibrate 160 mg tablet
On the label: Direct Rx. It's repackaged from NDC 68180-363, which isn't on any FDA listing we can find.
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 Direct Rx names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- tablet
- Strength
- 160 mg
- Approval
- ANDA ANDA204019
- On the market since
- Aug 9, 2019
- Package NDCs
72189-026-30- Official label
- DailyMed (National Library of Medicine), updated Jun 3, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?