NDC 50090-4561
Fenofibric Acid 135 mg capsule, delayed release
On the label: A-S Medication Solutions. It's repackaged from NDC 0115-1555, made by Amneal Pharmaceuticals of New York LLC (Fenofibric Acid). 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 relabels 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 A-S Medication Solutions names for other drugs.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, delayed release
- Strength
- 135 mg
- Approval
- NDA authorized generic NDA022224
- On the market since
- Sep 12, 2016
- Package NDCs
50090-4561-0- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2021
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?