Telmisartan And Hydrochlorothiazide Tablet
Product Images NDC 68180-193

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Telmisartan And Hydrochlorothiazide (NDC 68180-193). 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 the active ingredient Telmisartan, as depicted in the image showing its molecular framework with rings and side chains.*

FDA Label Image

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Chemical structure of Telmisartan showing the arrangement of its atoms and bonds including a sulfonamide group, a chlorine atom, and a benzene ring system.*

FDA Label Image

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An instructional diagram showing a hand pushing a tablet through a perforated blister pack to remove it. It demonstrates the method of extracting tablets from the packaging.*

FDA Label Image

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An illustration showing hands opening a small blister card or packet labeled Telmisartan and Hydrochlorothiazide Tablet 40 mg/12.5 mg, demonstrating how to peel back the foil to access the medication inside. The labeler Lupin Pharmaceuticals, Inc. is partially visible on the packaging.*

FDA Label Image

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An instructional illustration showing how to push a tablet out of a blister pack. The image features two hands holding the pack with an arrow indicating the direction to press the tablet for removal.*

FDA Label Image

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Label for Telmisartan and Hydrochlorothiazide Tablets USP 40 mg/12.5 mg, oral tablets in a 30 count package. The label includes the NDC 68180-193-06, manufacturer Lupin Pharmaceuticals, Inc., and storage instructions. The product is prescription only and states dosage details and barcode.*

FDA Label Image

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Label for Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg strength, oral tablet dosage form. The label indicates a quantity of 30 tablets, manufactured for Lupin Pharmaceuticals, Inc. The label includes NDC 68180-194-06, storage instructions, and manufacturer details including Lupin Limited in India.*

FDA Label Image

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Packaging label for Telmisartan and Hydrochlorothiazide Tablets USP, strength 80 mg/25 mg, oral tablet dosage form. The label states 30 tablets per package, manufactured by Lupin Pharmaceuticals, Inc. It includes storage instructions and details of the labeler Lupin Pharmaceuticals, Inc., Baltimore, Maryland, and manufacturer Lupin Limited, India.*

* 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.