Enalapril Maleate Tablet
Product Images NDC 50090-7222

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Enalapril Maleate (NDC 50090-7222). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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 the molecular components and arrangement of atoms and functional groups relevant to the active ingredient enalapril maleate.*

FDA Label Image

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A data table comparing incidence rates of various adverse effects leading to discontinuation for Enalapril maleate (n=573) and placebo (n=339). The effects are categorized by body system: Body As A Whole, Cardiovascular, Digestive, Nervous/Psychiatric, Respiratory, Skin, and Urogenital, with specific symptoms listed under each. Numeric incidence values for both Enalapril maleate and placebo are presented in two columns.*

FDA Label Image

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A table showing initial dosage recommendations of Enalapril maleate tablets related to renal status and creatinine clearance. Dosages vary from 5 mg to 2.5 mg per day based on kidney function, with specific notes for dialysis patients. The table includes renal function categories from normal to severe impairment.*

FDA Label Image

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Label for Enalapril maleate 5 mg oral tablets by A-S Medication Solutions, Libertyville, IL, NDC 50090-7222. The label advises storage at 68 to 77 degrees Fahrenheit, protection from moisture, and packaging information, including 30 tablets per container. The product number and a QR code are also visible.*

* 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.