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Fenofibric Acid Capsule, Delayed Release
Product Images NDC 69315-282
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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.
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Fenofibric Acid is a medication that comes in delayed-release capsules. Each capsule has choline fenofibrate equivalent to 45mg of fenofibric acid. It's a prescription-only medication, and it comes in 90 capsules per package. The package should be kept at 20°to 25° C (68° to 77° F) at a controlled room temperature according to USP. It is manufactured for Leading Pharma, LLC in the USA and is child-resistant. If the seal is broken or missing, do not use it. The package insert has all the instructions and relevant information. The manufacturer is Gravi Pharmaceuticals, based in Telangana-502307, INDIA. The Mfg. Lic. No. is 12/SRD/TS/2017/FIG 2, and the text was last revised in 12/2021.*
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This is a description of a medication called choline fenofibrate presented in delayed-release capsules. Each capsule contains fenofibric acid equivalent to 136 mg of fenofibric acid. The manufacturing company is Leading Pharma LLC with its location in Fairfield, NJ, and the packaging company is Graviti Pharmaceuticals Pvt. Ltd in India. The medication is for prescription-only and should be stored at a temperature of 20° to 25° C. The package contains 90 capsules and should be protected from moisture. The package is child-resistant and should not be used if the seal is broken.*
* 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.
