Fenofibrate Tablet
Product Images NDC 68180-231

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 68180-231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

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FDA Label Image

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This is a prescription medication called Fenofibrate. The usual dosage is not provided in the text and should be looked up in the prescribing information. There are 90 tablets per bottle and each tablet contains 54 milligrams of Fenofibrate USP. The medication should be stored at room temperature between 15°C-30°C (59°F-86°F). It is important to keep it away from the reach of children and to use child-resistant closure as required. The manufacturer is Lupin Pharmaceuticals Inc. located in Baltimore, Maryland. Code number MH/DRUGS/25-ND/59 is provided for identification.*

FDA Label Image

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This is a description of a medication called Fenofibrate. Each tablet contains 54 mg of fenofibrate and it is a USP drug. It is recommended to follow the instructions provided. The tablets should be stored at temperatures between 20°C to 25°C or 15°C to 30°C. The medication should be kept away from moisture and in a child-resistant container. It is important to keep this medication out of the reach of children. This medication is manufactured by Lupin Limited in Nagpur, India.*

FDA Label Image

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This is a prescription medicine called Fenofibrate Tablets USP, each film-coated tablet contains 54 mg of fenofibrate USP. The usual dosage should be seen in the accompanying prescribing information. The recommended storage temperature is between 15° to 30°C (59° to 86°F) and should be kept in a tight, light-resistant container and protected from moisture. This medicine should be kept out of reach of children, and it is not child-resistant. This medicine is manufactured by Lupin Limited in Goa, India, and was manufactured for Lupin Pharmaceuticals, Inc. in Baltimore, Maryland, United States.*

FDA Label Image

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The text describes a medication called Fenofibrate which is a film-coated tablet. The medication is used for certain medical conditions and contains 160 mg of fenofibrate USP. The dosage directions are available with prescription information. The medication should be stored between 15°C to 30°C (5 to 86°F) and should be protected from moisture. It should be kept out of reach of children and dispensed in a tight, light-resistant container. The medication is manufactured by Lupin Pharmaceuticals in Baltimore, Maryland and Lupin Limited in Nagpur, India.*

FDA Label Image

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This is a prescription drug called fenofibrate USP which is available in the form of 90 tablets with 160 mg of fenofibrate in each tablet. The recommended storage temperature for the tablets is 20°C to 25°C. The tablets can be stored at a higher temperature range between 15°C and 30°C. It is advised to store the tablets in a tight, light-resistant container with a child-resistant closure. This drug can only be obtained with an appropriate prescription. The manufacturer is Lupin Pharmaceuticals located in Baltimore, Maryland USA, and manufactured by Lupin Limited located in Nagpur, India.*

FDA Label Image

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This is a description for a medication called Fenofibrate Tablets USP, used in the treatment of high cholesterol and triglyceride levels. Each film-coated tablet contains 160 mg of fenofibrate USP. The usual dosage and storage instructions are given with the product. The medication should be stored at 25°C (77°F) and protected from moisture. The manufacturer of the medicine is Lupin Pharmaceuticals, and the tablets are made by Lupin Limited in Goa, India. For detailed prescribing information, consult the accompanying document.*

* 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.