Ertapenem Injection, Powder, Lyophilized, For Solution
Product Images NDC 0143-9429

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 Ertapenem (NDC 0143-9429). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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.

FDA Label Image

Image Of Ertapenem Sodium Chemical Structure (Ertapenem 01)

Image Of Ertapenem Sodium Chemical Structure (Ertapenem 01)
Chemical structure of ertapenem sodium, the active ingredient in Ertapenem injection powder for solution. The diagram shows the molecular arrangement with characteristic beta-lactam and carboxylate groups.*
FDA Label Image

Principal Display Panel (10 Single-dose vials Label)

Principal Display Panel (10 Single-dose vials Label)
Packaging label for Ertapenem 1 gram per vial injection by Hikma Pharmaceuticals USA Inc. The product is a lyophilized powder for solution, intended for intravenous or intramuscular use, with 10 single-dose vials per carton. The label includes dosage strength, NDC number 0143-9429-10, and manufacturer details.*
FDA Label Image

Principal Display Panel (1 Single-dose vial Label)

Principal Display Panel (1 Single-dose vial Label)
Label for Ertapenem 1 gram per vial injection powder, lyophilized, for solution. The label indicates it is for intravenous or intramuscular use, single-dose vial, manufactured by QILU Antibiotics Pharmaceutical Co., Ltd., for Hikma Pharmaceuticals USA Inc. The label includes lot and expiration date placeholders and a barcode.*

* 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.