Ampicillin Injection, Powder, For Solution
Product Images NDC 0404-9818
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Ampicillin (NDC 0404-9818). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Henry Schein, 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.
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The text is a table showing susceptibility test interpretive criteria for different pathogens. It displays information such as the disk diffusion zone diameter, minimal inhibitory concentration, and interpretive criteria for each pathogen. The table includes pathogens like Enterobacteriaceae, Enterococcsssp, Haemophius influenzae and parainencae, and Steplococcus.*
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This text appears to be a table of information regarding some medications or pharmaceuticals. It provides details like the name of the medication, the concentration, the amount of withdrawable, the claim diluent volume, and other information. The text seems to be incomplete and lacks context, making it hard to determine precisely what this table represents.*
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This text provides information on the stability period of various diluent concentrations under refrigerated and room temperature conditions. The stability period for diluents such as 0.9% Sodium Chloride Injection, USP, 5% Dextrose Injection, USP, Sterile Water for Injection, USP, and Lactated Ringer's Injection, USP, with varying concentrations are mentioned for specific time periods ranging from 1 hour to 72 hours. However, the last line appears to be incomplete due to errors.*
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This is a description of a vial of Ampicillin, a type of antibiotic. The vial is meant for direct intravenous administration and contains 2g of ampicillin in sodium USP equivalent. It is not made of rubber latex. The dry powder is to be stored at a controlled temperature between 68°F to TTF. The given lot number for this particular vial is H XXROOXKKK, and the expiry date is mentioned as mm—y¥ R o tRiNe. It also includes the manufacturer's information on the company, PharmaLLG, and the original manufacturing lot.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.