Bisoprolol Fumarate Tablet, Film Coated
Product Images NDC 72578-112

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bisoprolol Fumarate (NDC 72578-112). 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

Image (580d17c9 00d5 4fcf 8bc3 8e0dd5a330d2 01)

Image (580d17c9 00d5 4fcf 8bc3 8e0dd5a330d2 01)
Chemical structure of Bisoprolol Fumarate showing the molecular arrangement of bisoprolol with the fumarate salt component.*
FDA Label Image

5 mg (580d17c9 00d5 4fcf 8bc3 8e0dd5a330d2 02)

5 mg (580d17c9 00d5 4fcf 8bc3 8e0dd5a330d2 02)
Label for Bisoprolol Fumarate Tablets, USP 5 mg film-coated tablets. The unit-of-use package contains 30 tablets. Label displays the NDC 72578-111-06 and indicates Rx only. The product is labeled by Viona Pharmaceuticals Inc, with manufacturing by Cadila Healthcare Ltd, Ahmedabad, India. Storage and child safety instructions are included.*
FDA Label Image

10 mg (580d17c9 00d5 4fcf 8bc3 8e0dd5a330d2 03)

10 mg (580d17c9 00d5 4fcf 8bc3 8e0dd5a330d2 03)
Packaging label for Bisoprolol Fumarate Tablets USP 10 mg film-coated tablets. The label indicates a 30 tablet unit-of-use package, labeled Rx only. The labeler is Viona Pharmaceuticals Inc. Storage instructions and child-resistant packaging details are printed on the right side, along with manufacturer information from Cadila Healthcare Ltd, India, and distribution by Viona Pharmaceuticals Inc, Cranford, NJ. The NDC number 72578-112-06 is shown above the product name.*

* 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.