Fenofibrate Capsule
Product Images NDC 63304-444

4 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 63304-444). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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.

Product Images & Figures Index

FDA Label Image

130mg

130mg
Label for Fenofibrate Capsules, USP 130 mg oral capsules. The label shows a quantity of 30 capsules with the text RX only. The product is manufactured by Ohm Laboratories Inc. and distributed by Sun Pharmaceutical Industries, Inc. It includes storage instructions and two barcodes. The label features a blue block behind the strength and blue branding for Ohm.*
FDA Label Image

130mg (Image 01)

130mg (Image 01)
Label for Fenofibrate Capsules, USP 130 mg by Ohm Laboratories Inc. The label indicates the product is prescription-only and contains 90 capsules. It includes NDC 63304-444-90 and storage instructions. Manufactured by Ohm Laboratories, Inc. and distributed by Sun Pharmaceutical Industries, Inc.*
FDA Label Image

Structure 1 (Image 02)

Structure 1 (Image 02)
Fenofibrate Capsules, USP 43 mg oral capsules label by Sun Pharmaceutical Industries, Inc. The label includes the NDC number, dosage strength 43 mg, quantity of 30 capsules, and directions for use. It also displays barcodes and storage instructions.*
FDA Label Image

Structure

Structure
Chemical structure of fenofibrate, showing a chlorophenyl group connected to a carbonyl group and a diphenyl ether moiety, with an isopropyl ester substitution.*

* 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.