Bisoprolol Fumarate Tablet, Film Coated
Product Images NDC 65862-087

3 FDA label images from Aurobindo Pharma Limited · 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 65862-087). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (5 mg (30 Tablet Bottle))

Package Label-principal Display Panel (5 mg (30 Tablet Bottle))
Packaging label for Bisoprolol Fumarate Tablets USP, 5 mg, film-coated tablets, containing 30 tablets. The label shows the product is distributed by Aurobindo Pharma USA, Inc., and is labeled for prescription use only. Storage instructions, dosing guidance reference, and protection requirements are included on the label.*
FDA Label Image

Package Label-principal Display Panel (10 mg (30 Tablet Bottle))

Package Label-principal Display Panel (10 mg (30 Tablet Bottle))
Label for Bisoprolol Fumarate Tablets, USP 10 mg film-coated tablets by Aurobindo Pharma Limited. The label indicates a package size of 30 tablets and includes storage instructions, a barcode, and distributor information for Aurobindo Pharma USA, Inc.*
FDA Label Image

Chemical Structure (Bisoprolol Str)

Chemical Structure (Bisoprolol Str)
Chemical structure diagram showing the molecular structure of Bisoprolol Fumarate, including its bisoprolol moiety and fumarate component.*

* 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.