Nexletol Tablet, Film Coated
Product Images NDC 72426-118

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nexletol (NDC 72426-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Esperion Therapeutics, 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

Chemical Structure (Nexletol 01)

FDA Label Image

Figure 1 (Nexletol 02)

Figure 1 (Nexletol 02)
This text appears to be a report of a clinical trial comparing the effectiveness of Nexletol 180mg with Placebo in reducing LDL Cholesterol levels over a period of 36 weeks. The report displays the mean percent change in LDL Cholesterol levels at baseline and week 36 for the two groups of participants: one group received Nexletol 180mg while the other received a placebo. There were 10 subjects in the Nexletol group and 99 subjects in the Placebo group.*
FDA Label Image

Principal Display Panel (30 Tablet Bottle Label)

Principal Display Panel (30 Tablet Bottle Label)
This is information about the storage, dosage, and administration of a medication called NEXLETOL (bempedoic acid) fablefs. The package contains 30 tablets, each containing 180 mg of bempedoic acid. It is manufactured by Esperion Therapeutics, Inc. and should be stored at a temperature of 20°C to 25°C (68°F to 77°F), with excursions permitted to 15°C to 30°C (59°F to 86°F). The medication should be kept in the original package, and the desiccant should not be discarded. For more information on dosage and administration, consult the accompanying Package Insert.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.