Ertapenem Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-823

4 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ertapenem (NDC 63323-823). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi 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.

Product Images & Figures Index

FDA Label Image

Ert02 0002 01

Ert02 0002 01
Chemical structure of Ertapenem Sodium is shown in a two-dimensional molecular diagram, illustrating the arrangement of atoms and bonds characteristic of this antibiotic compound.*
FDA Label Image

Ert02 0002 02

Ert02 0002 02
Ertapenem 1 g injection, powder, lyophilized for solution vial label from Fresenius Kabi USA, LLC. The label includes the product name Ertapenem and identifies it as a lyophilized powder for intramuscular or intravenous injection in a 1 gram strength.*
FDA Label Image

Ert02 0002 03

Ert02 0002 03
Packaging label for Ertapenem Injection, 1 g per vial, by Fresenius Kabi USA, LLC. The label shows it's for intravenous or intramuscular use, includes 10 single-dose vials, and is labeled Rx only. The NDC 63323-823-20 is displayed along with branding.*
FDA Label Image

Ert02 0002 04

Ert02 0002 04
Label for Ertapenem injection, powder, lyophilized, for solution, 1 g per vial. The label indicates use for intravenous or intramuscular administration, single-dose vial, prescription only. It includes inactive ingredients and storage instructions. Manufactured for Fresenius Kabi USA, LLC, made in Italy.*

* 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.