Ampicillin Injection, Powder, For Solution
Product Images NDC 71872-7086

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ampicillin (NDC 71872-7086). 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 (7086)

This is a description of Ampicillin for Injection, a medication used for intramuscular or intravenous use. Each vial contains 1g of Ampicillin sodium USP and the sodium content of 583mg per 1g. The vial stopper is not made with natural rubber latex. The usual adult dosage is 250 to 500mg intramuscularly. The dry powder should be stored at 20 to 25°C. The accompanying insert should be read for detailed indications and precautions. This medication is manufactured in India and distributed by AuroMedics Pharma LLC.*

FDA Label Image

Package Label-principal Display Panel (1 g Container Label)

This vial contains 1 g of Ampicillin sodium for Intramuscular or Intravenous use. It should be added with a 35mL solvent to obtain a solution containing 250 mg of ampicillin per mL. Usual dosage is 250 to 500mg intramuscular every 6 hours. The detailed indications, dosage, and precautions can be found in the accompanying insert. The dry powder must be stored at 20° to 25°C. The product is distributed by AuroMedics Pharma LLC and made in India. The Batch and Expiry information are not available in the text.*

FDA Label Image

Chemical Structure (Ampicillin Str)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.