Bisoprolol Fumarate And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 0093-3243

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 0093-3243). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Bisoprolol Fumarate Structural Formula Image (Image 1)

Chemical structure diagram of bisoprolol fumarate and hydrochlorothiazide, showing molecular components linked to bisoprolol and fumarate groups.*

FDA Label Image

Hydrochlorothiazide Structural Image (Image 2)

Chemical structure of bisoprolol fumarate and hydrochlorothiazide, shown as a molecular diagram depicting rings, bonds, and functional groups including chloride, sulfonamide, and hydroxyl components.*

FDA Label Image

2.5 6.25 Label Impage (Image 3)

Label for Bisoprolol Fumarate and Hydrochlorothiazide Tablets, 2.5 mg/6.25 mg, film-coated tablets. The label indicates a package size of 100 tablets, distributed by Teva Pharmaceuticals USA, Inc. It includes storage instructions, dosage direction reference, and barcode. Manufactured in Bulgaria.*

FDA Label Image

Biso Hctz 5 (6.25mg label image)

Label for Bisoprolol Fumarate and Hydrochlorothiazide Tablets showing strength of 5 mg/6.25 mg. The label indicates the product contains 100 film-coated tablets, is Rx only, and is distributed by Teva Pharmaceuticals USA, Inc. It includes storage instructions, manufacturing location as Bulgaria, and has a barcode with NDC 0093-3242-01.*

FDA Label Image

Biso-hctz 10-6.25 Label Image (Image 5)

Label for Bisoprolol Fumarate and Hydrochlorothiazide Tablets, 10 mg/6.25 mg strength, film-coated tablets. The label states the NDC 0093-3243-56 and indicates dispensing details including storage temperature and manufacturer information, Teva Pharmaceuticals USA, Inc. The package contains 30 tablets and is marked Rx only.*

* 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.