Meropenem Injection, Powder, For Solution
Product Images NDC 70594-075

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 Meropenem (NDC 70594-075). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xellia Pharmaceuticals Usa 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

Chemical Structure (Meropenem 01)

Chemical Structure (Meropenem 01)
Chemical structure of meropenem dihydrate, showing its molecular arrangement including functional groups and hydration indicated by three water molecules.*
FDA Label Image

Principal Display Panel (500 mg Vial Carton)

Principal Display Panel (500 mg Vial Carton)
Packaging label for Meropenem for Injection, USP (I.V.) 500 mg/vial powder for solution injection by intravenous use. The label indicates a package size of 10 sterile vials, manufactured by Xellia Pharmaceuticals USA LLC. The label features prominent magenta bands with product name and strength, including instructions for intravenous use only and storage information.*
FDA Label Image

Principal Display Panel (1 g Vial Carton)

Principal Display Panel (1 g Vial Carton)
Packaging label for Meropenem for Injection, USP (I.V.) powder for solution, equivalent to 1 g meropenem per vial. The label indicates it is for intravenous use only and includes 10 x 1 g sterile vials. The label displays the labeler as Xellia Pharmaceuticals USA LLC and has a purple and white design with hexagonal graphic elements.*

* 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.