Fenofibrate Capsule
Product Images NDC 27241-120

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 27241-120). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ajanta Pharma Usa 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

Fenofibrate 134mg

Label for Fenofibrate Capsules, USP 134 mg by Ajanta Pharma USA Inc. The label indicates 100 oral capsules per container with NDC 27241-119-04. It includes storage instructions, child-resistant packaging details, and a barcode. The product is marketed by Ajanta Pharma USA Inc., Bridgewater, NJ, and made in India.*

FDA Label Image

Fenofibrate 200mg

Fenofibrate Capsules, USP 200 mg oral capsules label from Ajanta Pharma USA Inc. The label states the package contains 100 capsules and includes storage instructions, child-resistant packaging information, and a barcode. The product is marketed by Ajanta Pharma USA Inc., Bridgewater, NJ, and made in India.*

FDA Label Image

Fenofibrate 67mg

Fenofibrate Capsules, USP 67 mg oral capsule label from Ajanta Pharma USA Inc. The label indicates 100 capsules per bottle and includes storage instructions, child-resistant packaging information, and the requirement to keep medications out of children's reach. The label features the product name prominently with the strength highlighted in a brown box, alongside the NDC number 27241-118-04 and a barcode.*

FDA Label Image

Fenofibrate

Chemical structure of fenofibrate, showing rings and functional groups including chlorine, ester, and ketone moieties consistent with the fenofibrate molecule.*

* 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.