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Fenofibrate Capsule
Product Images NDC 68462-582
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 68462-582). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Glenmark Pharmaceuticals Inc., Usa, 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
Lbl134mg100s
Label for Fenofibrate Capsules USP 134 mg by Glenmark Pharmaceuticals Inc., USA. The label states Rx only, contains 100 capsules, and includes storage and child-resistant packaging warnings. Manufacturer information includes Glenmark Pharmaceuticals Limited, India, with distributor details for Glenmark Pharmaceuticals Inc., USA.*
Lbl200mg100s
Fenofibrate Capsules USP 200 mg oral capsules label by Glenmark Pharmaceuticals Inc. The label shows the NDC 68462-582-01 and states the product is prescription only with 100 capsules per container. It includes storage and handling information, manufacturer details from Glenmark Pharmaceuticals Limited in India, and the Glenmark logo.*
Lbl67mg100s
Label for fenofibrate capsules, USP, 67 mg strength. The label shows the product name, strength, and dosage form capsule. It is packaged by Glenmark Pharmaceuticals Limited, India, and manufactured for Glenmark Pharmaceuticals Inc., USA. The label states "Rx only" and the package count is 100 capsules. Storage and handling instructions, as well as contact information, are also present.*
Structure
Chemical structure of fenofibrate, showing its aromatic rings, carbonyl groups, and ester linkages typical of this active ingredient.*
* 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.
