Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mutual Pharmaceutical | Location not on file | Makes it and tests it | Not inspected on record |
| Mutual Pharmaceutical Company, Inc. | Location not on file | Makes it, packages it and labels it | Not inspected on record |
Recalls
- Oct 1, 2015 · Class III · Tribute Pharmaceuticals US Inc.
Chemical Contamination: The product may contain trace amounts of benzophenone, a component of the label varnish that may leach through the bottle and into the drug product.
Lots: Lot #: a) 6631401, Exp 03/16; b) 6631403, Exp 03/16; 6697001, Exp 06/17; c) 6631402, Exp 03/16; 6663401, Exp 10/16; 6697002, 6697004, Exp 06/17
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
- tablet
- Strength
- 35 mg
- Approval
- NDA NDA022418
- On the market since
- Aug 14, 2009
- Package NDCs
13310-101-0113310-101-0313310-101-0513310-101-0613310-101-0713310-101-1013310-101-90- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2013
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?