Enalapril Maleate Tablet
Product Images NDC 23155-704

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Enalapril Maleate (NDC 23155-704). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc., 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 diagram of Enalapril maleate showing its molecular composition, including aromatic rings, amide groups, and carboxylic acid functional groups.*

FDA Label Image

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A data table presenting the incidence of various adverse events leading to discontinuation among participants treated with Enalapril maleate compared to placebo. The table categorizes events by body system, including cardiovascular, digestive, nervous/psychiatric, respiratory, skin, and urogenital, with numeric incidence rates given for each group.*

FDA Label Image

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A dosing guideline table for Enalapril maleate showing initial daily doses based on renal status and creatinine clearance in mL/min. It categorizes renal function from normal to dialysis patients, with doses ranging from 5 mg for normal and mild impairment to 2.5 mg for moderate to severe impairment and dialysis days. Additional notes reference warnings and dosage adjustments based on blood pressure response on nondialysis days.*

FDA Label Image

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FDA Label Image

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Label for Enalapril Maleate Tablets USP 2.5 mg by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label shows a bottle containing 100 tablets. It includes storage instructions, dosage details, and warnings such as keeping the bottle tightly closed and out of reach of children. The label also includes a barcode and revision date of 12/2019.*

FDA Label Image

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Enalapril Maleate Tablets USP with a strength of 5 mg, in a package containing 100 tablets. The product is labeled for prescription use only (Rx only) and manufactured by Avet Pharmaceuticals Inc., a division of Heritage Pharmaceuticals Inc. The label includes dosage and storage information, a barcode, and manufacturer contact details.*

FDA Label Image

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Enalapril Maleate Tablets USP 10 mg bottle label showing the quantity of 100 tablets. The label includes dosage information, storage instructions, and cautionary statements. It is distributed by Avet Pharmaceuticals Inc., East Brunswick, NJ. The label features a barcode and specifies the product as prescription only, containing 10 mg enalapril maleate per tablet.*

FDA Label Image

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Label for Enalapril Maleate Tablets USP, 20 mg strength, containing 100 tablets. The label shows the proprietary name, strength, quantity, and manufacturer as Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. It includes storage instructions and warnings about child safety. The label includes a barcode and NDC 23155-707-01.*

FDA Label Image

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Enalapril Maleate Tablets USP 10 mg bottle label from Avet Pharmaceuticals Inc., containing 100 tablets. The label includes dosage instructions, storage conditions to keep at 20 to 25°C, and warnings to keep out of reach of children. The NDC code 23155-772-01 and barcode are also visible.*

FDA Label Image

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Label for Enalapril Maleate Tablets USP, 20 mg strength, distributed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label indicates 100 tablets in the container, prescription-only. It includes storage instructions, dosage directions, and warnings such as 'Keep container tightly closed' and 'Keep this and all medications out of the reach of children.' A barcode and NDC number 23155-773-01 are 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.