Bisoprolol Fumarate And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 72578-113

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Bisoprolol Fumarate And Hydrochlorothiazide (NDC 72578-113). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Viona 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 bisoprolol fumarate and hydrochlorothiazide. The image shows a molecular diagram with functional groups and bonds representing the combined chemical entities of bisoprolol and fumarate.*

FDA Label Image

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Chemical structure of bisoprolol fumarate, showing its molecular framework with chlorine, sulfur dioxide, and other functional groups clearly depicted.*

FDA Label Image

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Label for Bisoprolol Fumarate and Hydrochlorothiazide Tablets USP 2.5 mg/6.25 mg by Viona Pharmaceuticals Inc. The film-coated tablet package contains 30 tablets in a unit-of-use format. The label includes the NDC 72578-113-06, storage instructions, manufacturer and distributor information, and dosage strength prominently displayed.*

FDA Label Image

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Packaging label for Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP, 5 mg/6.25 mg strength. The label indicates 30 film-coated tablets in a unit-of-use package, labeled for prescription use only. The labeler is Viona Pharmaceuticals Inc, distributed from Cranford, NJ. The label includes storage instructions, dosage details, and child-resistant packaging information.*

FDA Label Image

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Packaging label for Bisoprolol Fumarate and Hydrochlorothiazide Tablets, USP 10 mg/6.25 mg, film-coated oral tablets. Label indicates a package of 30 tablets, unit-of-use, Rx only, by Viona Pharmaceuticals Inc. The label includes storage instructions, manufacturer Cadila Healthcare Ltd., and distributor information. National Drug Code (NDC) is 72578-115-06.*

* 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.