Bisoprolol Fumarate Tablet, Film Coated
Product Images NDC 16714-530

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bisoprolol Fumarate (NDC 16714-530). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

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

Packaging label for Bisoprolol Fumarate Tablets, USP 5 mg film-coated tablets. The label shows a package of 30 tablets, manufactured by Northstar Rx LLC and Aurobindo Pharma Limited, India. It includes storage instructions, dosage note, and a barcode with NDC 16714-529-01. The label also mentions protection from light and moisture.*

FDA Label Image

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

Label for Bisoprolol Fumarate Tablets, USP, 10 mg oral film-coated tablets. The package contains 30 tablets. The label includes manufacturer details for NorthStar Rx LLC and Aurobindo Pharma Limited, storage instructions, and dosage information. The NDC number is 16714-530-01.*

FDA Label Image

Chemical Structure (Bisoprolol Str)

Chemical structure of Bisoprolol Fumarate, showing the molecular components and arrangement of the active ingredient Bisoprolol Fumarate commonly used in pharmaceutical formulations.*

* 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.