Enalapril Maleate Tablet
Product Images NDC 23155-705

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Enalapril Maleate (NDC 23155-705). 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

Avet-logo (Avet Logo)

FDA Label Image

10 mg (37366051 Ccb9 4ce6 9060 0d4fa9e00a66 07)

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

20 mg (37366051 Ccb9 4ce6 9060 0d4fa9e00a66 08)

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

2-5mg-100s (2 5mg 100s)

Label for Enalapril Maleate Tablets USP 2.5 mg by Avet Pharmaceuticals Inc. The label indicates a bottle of 100 tablets, prescription only, with instructions emphasizing storage at controlled room temperature and keeping the medication out of children's reach. Includes NDC 23155-704-01 and a barcode.*

FDA Label Image

5mg-100s (5mg 100s)

Enalapril Maleate Tablets USP 5 mg tablet bottle label by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. The label states the strength as 5 mg with 100 tablets per bottle, marked as Rx only. It includes storage instructions for USP controlled room temperature and child-resistant container warnings, along with barcodes and revision date 11/2023.*

FDA Label Image

10mg-100s (10mg 100s)

Label for Enalapril Maleate Tablets USP, 10 mg strength, containing 100 tablets. The label shows that it is prescription-only, manufactured by Avet Pharmaceuticals Inc., a division of Heritage Pharmaceuticals Inc. It includes usage warnings, tamper-evident seal instructions, and a barcode.*

FDA Label Image

20mg-100s (20mg 100s)

Enalapril Maleate Tablets USP 20 mg label from Avet Pharmaceuticals Inc. The label indicates a package containing 100 tablets, prescription only. It includes storage instructions, a safety warning to keep medication out of reach of children, and the manufacturer details. Barcode and revision date (11/2023) 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.