Structure (D82243b9 3e56 4a2b 8750 Cb95ec106885 01)
Bisoprolol Fumarate
Product Images NDC 21695-670
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 21695-670). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Rebel Distributors Corp, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Bisoprolol Fumarate 5mg (D82243b9 3e56 4a2b 8750 Cb95ec106885 02)
This is a description of a medication bottle, containing Bisoprolol Fumarate 5mg tablets, with the product ID RB066730. Manufactured by Unichem Laboratories Ltd. in Goa, India, and distributed by Physician Partner in Thousand Oaks, CA. The tablets are pink, biconvex, round, and film-coated, with "UL" on one side and segmented with a "5" on the other. The medication should be stored at a controlled room temperature of 15°-30°C (59°-86°F) and kept out of reach of children.*
Bisoprolol Fumarate 10mg (D82243b9 3e56 4a2b 8750 Cb95ec106885 03)
This is a description of the medication Bisoprolol Fumarate 10mg in tablet form. The tablets are white and round, with "UL" on one side and "10" on the other, and they are film-coated. Each tablet contains 10mg of Bisoprolol Fumarate USP. The product is identified with the code RB067030 and is manufactured by Unichem Laboratories Ltd. located in Goa, India. It is distributed by Physician Partner located in Thousand Oaks, CA. The message "SO GO RO LRI ETE T I ERER TR W e i1 ) ep medication out of the reach of ch" is not readable and hence excluded from the description.*
* 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.
