Ampicillin Injection, Powder, For Solution
Product Images NDC 71872-7139

3 FDA label images from Medical Purchasing Solutions, Llc · 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 Ampicillin (NDC 71872-7139). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

Pdp (7139)

Pdp (7139)
Ampicillin for Injection, USP 2 g per vial powder for solution label. The label specifies contents for intravenous use, including ampicillin sodium equivalent to 2 g ampicillin per vial. Storage instructions, usage precautions, distributor (AuroMedics Pharma LLC), and repackager (Medical Purchasing Solutions, LLC) contact details are included. The vial is intended for single use, with sterile water for injection required for preparation.*
FDA Label Image

Package Label-principal Display Panel (2 g Container Label)

Package Label-principal Display Panel (2 g Container Label)
Ampicillin injection powder for solution, USP, 2 g per vial. The label indicates it is intended for intravenous use and distributed by AuroMedics Pharma LLC. The vial contains ampicillin sodium equivalent to 2 g ampicillin, with instructions for reconstitution with sterile water and storage at controlled room temperature (20-25°C). Rx only.*
FDA Label Image

Chemical Structure (Ampicillin Str)

Chemical Structure (Ampicillin Str)
Chemical structure of Ampicillin Sodium, showing the molecular arrangement including a phenyl group, amide linkage, and beta-lactam ring as part of the antibiotic's core structure.*

* 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.