Enalapril Maleate Tablet
Product Images NDC 51655-110

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 Enalapril Maleate (NDC 51655-110). 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, depicting molecular components including a phenyl group, ethyl ester, amide linkage, and a carboxyl functional group, consistent with the active ingredient in the product.*
FDA Label Image

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A data table comparing incidence rates of adverse events between Enalapril maleate (n=573) and placebo (n=339). Events are categorized by body system including Body As A Whole, Cardiovascular, Digestive, Nervous/Psychiatric, Respiratory, Skin, and Urogenital, with incidence percentages listed for each treatment group.*
FDA Label Image

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A dosage adjustment table for Enalapril maleate tablets showing initial doses in mg/day based on renal status and creatinine clearance. It includes dosing recommendations for normal renal function, mild impairment, moderate to severe impairment, and dialysis patients with clarifying footnotes about warnings and dosage adjustments.*
FDA Label Image

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FDA Label Image

Label (51655 110 26)

Label (51655 110 26)
Label for Enalapril Maleate tablets, USP 5 mg, containing 90 tablets. The label includes storage instructions at 20°-25°C and warns to keep out of reach of children. It shows the product NDC 51655-110-26 and identifies Northwind Pharmaceuticals as the repackager and Northwind Health Company, LLC as the labeler.*

* 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.