Chemical Structure (Soliqua 01)
Soliqua 100/33 Injection, Solution
Product Images NDC 0024-5761
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Product Visual Gallery
This gallery contains 25 technical images submitted to the FDA as part of the official labeling for Soliqua 100/33 (NDC 0024-5761). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Sanofi-aventis U.s. 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.
Product Images & Figures Index
Chemical Structure (Soliqua 02)
This is a list of body parts including upper arms, stomach and thighs. It does not provide any further context or information.*
Image (Soliqua 03)
The text describes the design of a medication injection device. It includes a dose selector, rubber seal, medicine scale, medicine name, injection button, and a note that the plunger will not be visible until a few doses have been administered. The text also mentions the expiration date being located on the back.*
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SOLIQUA® 100/33 is a prescription injection medication consisting of 100 units/mL insulin glargine and 33 mcg/mL lixisenatide. It is intended solely for subcutaneous injections and for single patient use only. SOLIQUA® 100/33 should be refrigerated at 36°F to 46°F (2C to 8°C) prior to first use, and protected from light. After first use, the pen should be stored at room temperature up to 77°F (25°C) for 28 days before disposal. A medication guide and secure sticker should be included by the supplier. Needles sold by separate manufacturers are compatible. Dosage adjustments should be made cautiously under medical supervision, and its use is not recommended for pregnant or nursing women without appropriate professional advice. Keep out of reach of children.*
* 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.
