Enalapril Maleate Tablet
Product Images NDC 51655-058

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 51655-058). 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 depicting the molecular formula of enalapril maleate, showing the connectivity of its component atoms and functional groups clearly.*
FDA Label Image

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A data table comparing the incidence rates of various adverse effects and discontinuation rates between Enalapril maleate (n=673) and placebo (n=339) across several body systems including Body As A Whole, Cardiovascular, Digestive, Nervous/Psychiatric, Respiratory, Skin, and Urogenital. The table lists specific conditions like orthostatic effects, syncope, dizziness, cough, and urinary tract infection with corresponding numerical incidence values for both groups.*
FDA Label Image

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A dosing table for Enalapril maleate tablets showing recommended initial doses based on renal function. The table lists renal status categories (Normal, Mild Impairment, Moderate to Severe Impairment, Dialysis Patients) with corresponding creatinine clearance levels and suggested initial dose in mg per day. It includes notes about anaphylactoid reactions and dosage adjustments on nondialysis days.*
FDA Label Image

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FDA Label Image

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Label for Enalapril Maleate Tablets USP 20 mg, containing 90 tablets. The label includes the NDC 51655-058-26 and indicates the product is prescription only (Rx only). Storage instructions advise keeping the container tightly closed and protecting from moisture, with recommended storage at 20°-25°C (68°-77°F). 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.