NDC 50090-6120
fenofibrate 134 mg capsule
On the label: A-S Medication Solutions. It's repackaged: A-S Medication Solutions rebottles it from Glenmark Pharmaceuticals Inc., USA's NDC 68462-581.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Glenmark Pharmaceuticals Limited | Dhar, India | Makes it and tests it | Serious problems, FDA actionFeb 14, 2025 · 8 inspections, 1 with FDA action |
Repackaging site
- A-S Medication Solutions LLC, Libertyville, IL, United States · repackages it and relabels it
Recalls
- Mar 13, 2025 · Class II · Glenmark Pharmaceuticals Inc., USA
CGMP Deviations
Lots: Lot # 17230834, exp. date Mar-25 17230835, exp. date Mar-25
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Fenofibric Acid: every company that makes it
- Form
- capsule, oral
- Strength
- 134 mg
- Approval
- ANDA ANDA205566
- On the market since
- Apr 7, 2017
- Package NDCs
50090-6120-0- Official label
- DailyMed (National Library of Medicine), updated Nov 1, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?