Fenofibric Acid Capsule, Delayed Release
Product Images NDC 69315-282

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fenofibric Acid (NDC 69315-282). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leading Pharma, Llc, 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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Chemical structure diagram of fenofibric acid with a chlorine-substituted aromatic ring and other functional groups, consistent with the active ingredient fenofibric acid.*

FDA Label Image

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Label for Fenofibric Acid Delayed-Release Capsules containing 45 mg strength. The package contains 90 capsules. The label includes the NDC number 69315-281-09 and states the drug is prescription only. It shows the labeler as Leading Pharma, LLC and mentions manufacturing by Graviti Pharmaceuticals Pvt. Ltd. Storage instructions and warnings about moisture and child-resistant packaging are also included.*

FDA Label Image

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Label for Fenofibric Acid Delayed-Release Capsules 135 mg, oral capsules, 90 count. The label shows the product name, strength, and quantity with the labeler Leading Pharma, LLC. It includes storage instructions, manufacturer information (Graviti Pharmaceuticals Pvt. Ltd., India), and warnings about moisture protection and child resistance. A barcode and NDC number 69315-282-09 are visible.*

* 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.