Fibricor
Product Images NDC 70347-035

3 FDA label images from Aralez Pharmaceuticals Us Inc. · 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 Fibricor (NDC 70347-035). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aralez Pharmaceuticals Us 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

Fibricor 105 mg Tablet (Fibricor 105)

Fibricor 105 mg Tablet (Fibricor 105)
FIBRICOR 105 mg (fenofibric acid) tablets label showing a bottle containing 30 tablets. Manufactured by Aralez Pharmaceuticals US Inc., it indicates each tablet contains 105 mg fenofibric acid and is dispensed in a light-resistant container. Storage instructions specify temperature control between 20° to 25°C (68° to 77°F). The label includes a barcode and a note to see the package insert for full prescribing information.*
FDA Label Image

Fibricor 35 mg Tablet (Fibricor 35)

Fibricor 35 mg Tablet (Fibricor 35)
FIBRICOR 35 mg tablets by Aralez Pharmaceuticals US Inc. The label indicates fenofibric acid as the active ingredient, with a 30-tablet count. It includes storage instructions and a barcode, emphasizing the product is Rx only and contains light-resistant packaging.*
FDA Label Image

Structural Formula (Structural Formula)

Structural Formula (Structural Formula)
Chemical structure diagram depicting the active ingredient in FIBRICOR by Aralez Pharmaceuticals US Inc. The structure includes a chlorophenyl group, two benzene rings, and a carboxylic acid group attached to a tert-butyl substituent.*

* 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.