Lisinopril And Hydrochlorothiazide Tablet
Product Images NDC 68180-520

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lisinopril And Hydrochlorothiazide (NDC 68180-520). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin 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 the active ingredient Lisinopril, illustrating its molecular arrangement including functional groups and hydration state.*

FDA Label Image

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Chemical structure diagram of Hydrochlorothiazide, one of the active ingredients in Lisinopril and Hydrochlorothiazide tablets by Lupin Pharmaceuticals, Inc. The structure shows the arrangement of atoms including sulfur, chlorine, nitrogen, oxygen, and carbon.*

FDA Label Image

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Label for Lisinopril and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg strength, manufactured by Lupin Pharmaceuticals, Inc. The label states each tablet contains 10 mg Lisinopril and 12.5 mg Hydrochlorothiazide, with a package size of 100 tablets. Storage instructions specify keeping the product at 20° to 25°C and protecting from excessive light and humidity. The label includes the NDC 68180-518-01 and barcode.*

FDA Label Image

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Label for Lisinopril and Hydrochlorothiazide Tablets USP 20 mg/12.5 mg, 100 count, oral tablet by Lupin Pharmaceuticals, Inc. The label shows active ingredients and strengths, storage instructions, and manufacturer information.*

FDA Label Image

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Label for Lisinopril and Hydrochlorothiazide Tablets USP, 20 mg/25 mg strength. The tablet form is oral. The label includes packaging details indicating 100 tablets per package, manufacturer Lupin Pharmaceuticals, Inc., and storage instructions to protect from excessive light and humidity at 20°C to 25°C. The label shows an NDC of 68180-520-01 and a barcode.*

* 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.