Fenofibric Acid
Product Images NDC 72834-035

3 FDA label images from Sarras Health, Llc · 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 Fenofibric Acid (NDC 72834-035). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sarras Health, Llc, 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

Fenofibric Acid 105 mg Tablet (Fenofibric Acid 105)

Fenofibric Acid 105 mg Tablet (Fenofibric Acid 105)
Label for Fenofibric Acid Tablets, each containing 105 mg of active ingredient. The label includes storage instructions (20° to 25°C), dispensing directions, and tablet identification (debossed: AR 788). The product is distributed by Sarras Health, LLC, Athens, GA. It contains 15 tablets and highlights Non-Varnish Serialization. A barcode and the NDC 72834-105-15 are also visible.*
FDA Label Image

Fenofibric Acid 35 mg Tablet (Fenofibric Acid 35)

Fenofibric Acid 35 mg Tablet (Fenofibric Acid 35)
Label for Fenofibric Acid Tablets 35 mg by Sarras Health, LLC. The label includes dosage strength, quantity of 30 tablets, storage instructions at 20-25°C, and a barcode. It notes the tablet is debossed with AR 787 and indicates the product is for prescription use only with non-varnish serialization.*
FDA Label Image

Structural Formula (Structural Formula)

Structural Formula (Structural Formula)
Chemical structure of fenofibric acid, an active pharmaceutical ingredient. The diagram shows benzene rings with chlorine, ketone, ether, and carboxylic acid groups, consistent with fenofibric acid's molecular framework.*

* 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.