Losartan Potassium And Hydrochlorothiazide Tablet
Product Images NDC 68180-217

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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Chemical structure of Losartan Potassium and Hydrochlorothiazide showing the molecular arrangement and potassium ion (K+). This diagram depicts the active ingredients' chemical framework as part of the pharmaceutical product.*

FDA Label Image

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Chemical structure diagram of Losartan Potassium and Hydrochlorothiazide, showing molecular bonds and functional groups including a sulfonamide and chlorine substitution on a benzene ring.*

FDA Label Image

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Label for Losartan Potassium and Hydrochlorothiazide Tablets USP 50 mg/12.5 mg by Lupin Pharmaceuticals, Inc. The package contains 30 film-coated tablets. It includes dosage and storage instructions, manufacturer information, and a barcode. Produced by Lupin Limited in India for Lupin Pharmaceuticals in the US.*

FDA Label Image

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Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, 50 mg/12.5 mg strength, oral tablet dosage form. The label states it is manufactured for Lupin Pharmaceuticals, Inc., and manufactured by Lupin Limited in India. The package contains 30 film-coated tablets and includes storage instructions and dosage reference. A barcode and space for lot number and expiration date are also visible.*

FDA Label Image

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Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/12.5 mg strength, oral tablet form. The label displays the quantity of 30 tablets and shows Lupin Pharmaceuticals, Inc. as the manufacturer. It includes dosage storage instructions, a barcode, and notes the product is prescription only.*

FDA Label Image

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Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, strength 100 mg/12.5 mg, oral tablets. The label indicates each film-coated tablet contains 100 mg losartan potassium and 12.5 mg hydrochlorothiazide. Pack contains 30 tablets. Manufactured for Lupin Pharmaceuticals, Inc., Baltimore, Maryland, and by Lupin Limited, India. Storage instructions and barcode included.*

FDA Label Image

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Label for Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg tablets USP by Lupin Pharmaceuticals, Inc. The label indicates a pack size of 30 film-coated tablets. It includes storage instructions, a barcode, manufacturer details, and states the product is Rx only.*

FDA Label Image

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Label for Losartan Potassium and Hydrochlorothiazide Tablets USP, 100 mg/25 mg strength, oral tablet form, containing 30 tablets. The label indicates it is a prescription drug manufactured by Lupin Pharmaceuticals, Inc. Storage instructions and dosage advisory are also provided on the label along with a barcode and lot/expiration date fields.*

* 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.