Product Images Fenofibric Acid Delayed-release
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Product Label Images
The following 3 images provide visual information about the product associated with Fenofibric Acid Delayed-release NDC 69844-023 by Graviti Pharmaceuticals Private Limited, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
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Each capsule of the delayed-release type contains 45mg of fenofibric acid equivalent to choline fenofibrate. It is necessary to refer to the package insert for full prescribing information. The product must be stored in temperatures ranging from 20 to 25°C, in a location protected from moisture. The package is resistant to children and for safety do not accept the product if the seal over the bottle's opening is broken or missing. The product Gravt Pharmaceuticals was manufactured in Wilmington, Delaware, USA, while Gravt Pharmaceuticals Pvt. L. manufactured it in Tlangana-502307, INDIA. The product is only for Rx use with an NDC 89844-022.01 code, and the pack holds 30 capsules.*
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Each delayed-release capsule contains choline fenofibrate equivalent to fenofibric acid of 135mg. This medication is used for the treatment of high cholesterol and triglyceride levels. The package insert should be consulted for full prescribing information. The manufacturer is Gravt Pharmaceuticals Inc. in Wilmington, Delaware, and the capsules are made resistant to children. This medication should not be accepted if the package cover is broken or open. The package also shows that it contains 30 capsules.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.