Bisoprolol Fumarate Tablet
Product Images NDC 43547-617

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bisoprolol Fumarate (NDC 43547-617). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solco Healthcare Us, Llc, 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

Structure (Image 01)

Structure (Image 01)
Chemical structure of bisoprolol fumarate, showing the bisoprolol molecule paired with fumaric acid. The diagram depicts the molecular arrangement of atoms and bonds characteristic of bisoprolol fumarate.*
FDA Label Image

5 (Image 02)

5 (Image 02)
Packaging label for Bisoprolol Fumarate Tablets, USP 5 mg oral tablets, containing 30 tablets per unit-of-use package. Label shows NDC 43547-616-03 and indicates prescription use only. Manufactured by Prinston Laboratories and distributed by Solco Healthcare US, LLC. Includes storage instructions and barcode on the right side.*
FDA Label Image

10 (Image 03)

10 (Image 03)
Packaging label for Bisoprolol Fumarate Tablets USP 10 mg, oral tablets supplied in a container of 30 tablets. The label shows the product name, strength, and quantity, with a blue and white color scheme and a graphic element. It includes the NDC number 43547-617-03 and states the product is Rx only. The labeler is Solco Healthcare US, LLC, with manufacturing by Prinston Laboratories. Storage instructions and other regulatory information appear on the label.*

* 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.