Ampicillin Injection, Powder, For Solution
Product Images NDC 71872-7249

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 Ampicillin (NDC 71872-7249). 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

71872-7249-1.pdp (71872 7249 1)

71872-7249-1.pdp (71872 7249 1)
Text panel for Ampicillin for Injection, USP powder for solution with an active equivalent to 1 gram ampicillin per vial. It includes instructions for IM or IV use, dosing guidance for children and adults, storage conditions at 20° to 25°C, and manufacturing information with lot and expiration placeholders. Distributed by Medical Purchasing Solutions, Scottsdale, AZ.*
FDA Label Image

Chemical Structure (Image 01)

Chemical Structure (Image 01)
Chemical structure diagram of the active ingredient Ampicillin. The diagram shows the detailed molecular structure including a beta-lactam ring, side chains, and sodium salt form (COONa). This structure represents the Penicillin class antibiotic used for injection as a powder for solution.*
FDA Label Image

Ampicillin 1 Gram Vial Label (Image 06)

Ampicillin 1 Gram Vial Label (Image 06)
Ampicillin for Injection, USP 1 gram powder for solution in a vial label. The label shows the active ingredient as ampicillin sodium equivalent to 1 gram ampicillin. It indicates use for intramuscular (IM) or intravenous (IV) injection and is marked Rx only. The label includes dosage and reconstitution instructions, a barcode, and the manufacturer Medical Purchasing Solutions, LLC.*

* 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.