Fenofibrate Tablet
Product Images NDC 70518-2907

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 70518-2907). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

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FDA Label Image

Fenofibrate 160mg 70518 2907 01

Fenofibrate is a prescription drug manufactured by LifeStar at their facility in Mahwah, NJ 07430. It is available in a package with an NDC number of 70518-2907-01, and a source NDC of 70756-0215-51. The medication should be stored between 20-26°C (63-77°F) and should be kept away from children. The package insert should be consulted for directions for use. The drug has been repackaged by RemedyRepack Inc. in Indiana, PA 15701, with a contact number of 724.466.8762.*

FDA Label Image

Remedy_label (Remedy Label)

Fenofibrate is a medication that requires a prescription. It comes in packaging with the NDC number 70518-2907-00 and an undisclosed expiration date and lot number. The source NDC for this drug is 70756-0215-90, and it is manufactured by LifeStar in Mahwah, NJ. People who have this medication are advised to keep it away from children. Information about how to take the medication can be found in the package insert. The drug should be stored at a temperature of 20-26°C (63-77°F) with permitted excursions to 15-30°C (59-86°F) according to USP guidelines. This particular package was repackaged by RemedyRepack Inc. in Indiana, PA.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.