Losartan Potassium And Hydrochlorothiazide Tablet
Product Images NDC 68180-217

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Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 68180-217). 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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FDA Label Image

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FDA Label Image

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This is a medication package for Losartan Potassium and Hydrochlorothiazide tablets manufactured by Lupin Pharmaceuticals, Inc. The package contains 30 film-coated tablets, with each tablet containing 50mg of Losartan potassium and 12.5mg of Hydrochiorothiazide. The recommended adult dosage is not available in the given text.*
FDA Label Image

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This is a description of a medication - Losartan and Hydrochlorothiazide tablets. It includes the NDC number, prescribed dosage information, storage information and the manufacturer's details. Each tablet contains Losartan potassium USP of 50mg and Hydrochlorothiazide USP of 2.5mg. It is manufactured by Lupin Pharmaceuticals and is only available under prescription.*
FDA Label Image

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Losartan potassium and Hydrochlorothiazide Tablets USP ML 2582010 is a medication that comes in a container that must be kept tightly closed and protected from light. The usual adult dosage is not available in this text, so it is recommended to see the prescribing information. Each film-coated tablet contains 100 mo. of Losartan potassium USP (amorphous) and 12.5 g of Hydrochlorothiazide USP. It is manufactured by Lupin Pharmaceuticals in India and must be stored at a controlled room temperature between 59°F to 86°F. This medication is available only with a prescription. The dimensions of the unvarnished area on the container are 54 mm x 16 mm.*
FDA Label Image

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Losartan potassium and Hydrochlorothiazide USP are contained in each film-coated tablet manufactured by Lupin Pharmaceuticals for adult use. The usual adult dosage must be seen from the accompanied prescribing information. It is recommended to store the tablets at room temperature, and to protect the container from excursions, keeping it tightly closed. The tablets come in a package of 30 and each has Losartan potassium USP (amorphous) of 100mg and Hydrochlorothiazide USP of 12.5mg. The manufacturer is Lupin Limited based in India while Lupin Pharmaceuticals Inc, based in Baltimore, Maryland, is one of its distributors located in the United States.*
FDA Label Image

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This is a description of a medication called Losartan Potassium with Hydrochlorothiazide, provided in tablet form. The usual adult dosage is not specified within the given text, and it is advised to refer to the accompanying prescribing information. The medication is manufactured by Lupin Pharmaceuticals, Inc. and should be stored at a temperature between 15-30°C. The container should be tightly closed and kept away from light. The tablets are manufactured in India and each film-coated tablet contains 100mg of Losartan potassium USP and 25mg of Hydrochlorothiazide USP. The product is available in a container of 30 tablets and requires a prescription (Rx only).*
FDA Label Image

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This is a medication description for Losartan and Hydrochlorothiazide tablets manufactured by Lupin Pharmaceuticals. The usual adult dosage information is not available and the tablets must be stored at room temperature. Each film-coated tablet contains 100mg of Losartan potassium and 25mg of Hydrochlorothiazide. The product is available in a container that needs to be tightly closed and protected from light. The manufacturer is located in Baltimore, Maryland, United States.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.