Valsartan And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 68180-103

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Valsartan And Hydrochlorothiazide (NDC 68180-103). 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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Four graphs display the probability of achieving specific systolic and diastolic blood pressure targets at Week 8 for Valsartan and Hydrochlorothiazide, Valsartan alone (160 mg/320 mg), Hydrochlorothiazide alone (25 mg), and placebo. Each graph plots probability percentages against baseline systolic or diastolic blood pressure values.*

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Chemical structure diagram of Valsartan, one of the active ingredients in the Valsartan and Hydrochlorothiazide medication. The image shows the molecular arrangement including various functional groups and rings characteristic of Valsartan.*

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Chemical structure of valsartan and hydrochlorothiazide, depicted as a molecular diagram showing atoms and bonds characteristic of these active ingredients in the tablet.*

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Label for Valsartan and Hydrochlorothiazide Tablets USP, 80 mg / 12.5 mg, film-coated tablets. The label indicates 90 tablets per container, manufactured for Lupin Pharmaceuticals, Inc., Baltimore, MD, and manufactured by Lupin Limited, Goa, India. Storage and handling instructions are included, and the product is Rx only.*

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Packaging label for Valsartan and Hydrochlorothiazide 80 mg/12.5 mg film-coated tablets. The label shows the product name, strength, dosage form, oral route, and Lupin Pharmaceuticals, Inc. as the labeler. The design features orange and white colors with text detailing the product and usage restrictions such as 'Rx only.'*

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP 80 mg/12.5 mg, film-coated tablets. The label states Rx only and shows a package quantity of 100 tablets (10 x 10 unit-dose), manufactured for Lupin Pharmaceuticals, Inc., Baltimore, Maryland, and manufactured by Lupin Limited, Goa, India. The label includes storage instructions and active ingredient amounts per tablet.*

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Label for Valsartan and Hydrochlorothiazide Tablets USP 160 mg/12.5 mg by Lupin Pharmaceuticals, Inc. The film-coated tablets come in a 90-count package. The label includes storage instructions, dosage note to see prescribing information, and manufacturer details including Lupin Limited, Goa, India.*

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP, 160 mg/12.5 mg, by Lupin Pharmaceuticals, Inc. The label includes multiple panels with dosage strength, product name, and manufacturer information, designed for film-coated oral tablets.*

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP, 160 mg/12.5 mg, film-coated oral tablets. The label states the product contains 100 tablets (10 x 10 unit-dose) and is manufactured by Lupin Pharmaceuticals, Inc. with manufacturing from Lupin Limited, India. It includes storage instructions and a barcode for scanning.*

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Label for Valsartan and Hydrochlorothiazide Tablets USP 160 mg/25 mg film-coated tablets. The label indicates a package of 90 tablets, manufactured for Lupin Pharmaceuticals, Inc., with storage instructions and usual dosage advisory. The label also includes the NDC 68180-105-09 and details about the manufacturer Lupin Limited in India.*

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Box and carton labels for Valsartan and Hydrochlorothiazide tablets USP 160 mg/25 mg from Lupin Pharmaceuticals, Inc. The film-coated tablets come in oral dosage form with packaging showing multiple panels including drug name, strengths, labeler name, and usage instruction parts of the label.*

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP, 160 mg/25 mg, film-coated oral tablets. The label shows the product name, strength, Rx only status, manufacturer Lupin Pharmaceuticals, Inc., and contains 100 tablets (10 x 10 unit-dose). Storage instructions and manufacturing details are also visible on the label.*

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Label for Valsartan and Hydrochlorothiazide Tablets USP, 320 mg/12.5 mg, film-coated tablets by Lupin Pharmaceuticals, Inc. The label shows the 90 tablets count, storage instructions, active ingredient amounts per tablet, manufacturer details, and barcode. The product is prescription-only.*

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP, 320 mg/12.5 mg strength, film-coated oral tablets. The label includes the proprietary and generic names, manufacturer Lupin Pharmaceuticals, Inc., dosage form, and strengths prominently displayed. The label is primarily blue and white with detailed regulatory text and barcodes.*

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Package label for Valsartan and Hydrochlorothiazide Tablets USP 320 mg/12.5 mg, film-coated tablets. The label shows the product name, strength, and dosage form. It includes the quantity of 100 tablets (10 x 10 unit-dose) and indicates prescription use only. The labeler is Lupin Pharmaceuticals, Inc., with manufacturing details for Lupin Limited, India. Storage and handling instructions are printed, along with the NDC number 68180-101-13 and a barcode.*

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Label for Valsartan and Hydrochlorothiazide Tablets USP 320 mg/25 mg by Lupin Pharmaceuticals, Inc. The film-coated tablet label shows a package size of 90 tablets. It lists active ingredients with strengths (valsartan 320 mg, hydrochlorothiazide 25 mg) and includes storage instructions, manufacturer details, and an NDC barcode.*

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP, 320 mg/25 mg strength, film-coated tablets for oral use. The label includes drug name, strength, form, manufacturer Lupin Pharmaceuticals, Inc., and NDC information on a white and red background.*

FDA Label Image

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Packaging label for Valsartan and Hydrochlorothiazide Tablets USP, 320 mg/25 mg strength, film-coated oral tablets. The label shows a 100-tablet count (10 x 10 unit-dose) by Lupin Pharmaceuticals, Inc. The label includes storage instructions, dosage directions to see accompanying information, and manufacturer details for Lupin Limited, Goa, India. The National Drug Code (NDC) is 68180-102-13.*

* 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.