48 mg 30 Tablets (Image 01)
Fenofibrate Tablet, Film Coated
Product Images NDC 63304-449
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 63304-449). 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.
48 mg 90 Count (Image 02)
48 mg 500 Tablets (Image 03)
This is a description of medication named "Tablets, USP". Each tablet contains 48 mg of the active ingredient. This medication is available with a prescription and is manufactured by Sun Pharmaceutical Industries, located in Cranbury, NJ. The rest of the texts are not available in English.*
145 mg 30 Tablets (Image 04)
This is a description of a medication identified as Fenofibrate made in tablet form. It comes in a bottle containing 500 tablets and is only available with a prescription. A lot number is indicated, however, the content of the lot is not provided. There is also a reference to a non-varnish area, although it is unclear what that means in relation to the medication.*
145 mg 90 Count (Image 05)
This bottle contains 30 tablets of Fenofibrate, USP 145 mg, with the National Drug Code (NDC) of 63304-449-30. The indicated pharmaceutical company is Pharma's Sun. The rest of the text seems to be unreadable.*
145 mg 500 Tablets (Image 06)
This is a medication called Fenofibrate, available in tablet form with a strength of 145 micrograms. It comes in a bottle with 90 tablets and requires a prescription to obtain. There may be an image or graphic on the packaging that does not include varnish.*
Image 07
This is a medication package for Fenofibrate, a drug used to lower high levels of cholesterol and triglycerides in the blood. The package contains 500 tablets with each tablet containing 145mg of Fenofibrate. The drug is available only with a prescription (Rx only). The mentioned NDC (National Drug Code) can be used by healthcare providers and pharmacists to identify the drug product.*
* 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.
