Enalapril Maleate Tablet
Product Images NDC 51655-006

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Enalapril Maleate (NDC 51655-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northwind Health Company, 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 of Enalapril maleate showing its molecular components and bonding arrangement as presented in the image.*

FDA Label Image

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Table presenting the incidence rates of adverse effects leading to discontinuation in patients treated with Enalapril maleate 10 mg tablets compared to placebo. The events are categorized by body system, including cardiovascular, digestive, nervous/psychiatric, respiratory, skin, and urogenital, showing percentages of occurrence and discontinuation incidence for each group.*

FDA Label Image

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A data table detailing initial dosage recommendations of Enalapril maleate based on renal status and creatinine clearance. Dosage varies from 5 mg to 2.5 mg daily, with specific adjustments for dialysis patients. Notes reference warnings about anaphylactoid reactions and dosage adjustments based on blood pressure response.*

FDA Label Image

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FDA Label Image

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Label for Enalapril Maleate Tablets USP 10 mg, containing 90 tablets, labeled Rx Only. The label includes storage instructions to keep at 20°-25°C (68°-77°F) in original container, tightly closed, and protected from moisture. The labeler is Northwind Health Company, LLC.*

* 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.