Meropenem Injection, Powder, For Solution
Product Images NDC 0409-1391

3 FDA label images from Hospira, Inc. · 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 0409-1391). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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.

Product Images & Figures Index

FDA Label Image

Structure (Image 01)

Structure (Image 01)
Chemical structure of Meropenem, showing its molecular formula with labeled atoms and bonds, including a carboxyl group, sulfur atom, and dimethylamine side chain, consistent with the active ingredient Meropenem.*
FDA Label Image

Meropenem 500 mg Vial Label (Image 02)

Meropenem 500 mg Vial Label (Image 02)
Meropenem 500 mg/10 mL injection powder for solution vial label by Hospira, Inc. The label states each vial contains meropenem equivalent to 500 mg meropenem activity, sodium content approximately 45.1 mg. The vial is for intravenous use only, sterile, and prescription use. Preparation instructions include dilution and storage temperature guidelines with a barcode and lot/expiration date area visible.*
FDA Label Image

Meropenem 1 Gram Vial Label (Image 03)

Meropenem 1 Gram Vial Label (Image 03)
Meropenem injection powder label for intravenous use, 1 gram per vial by Hospira, Inc. Each vial contains meropenem equivalent to 1 gram of meropenem activity with sodium content of approximately 90.2 mg. The label includes instructions for preparation and storage, and indicates the product is sterile and prescription-only.*

* 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.