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.

FDA Label Image

Formula1.jpg (Formula1)

Formula1.jpg (Formula1)
Chemical structure diagram of ampicillin sodium, showing its molecular framework with key functional groups including a beta-lactam ring, an amide linkage, and a phenyl group.*
FDA Label Image

Image1.jpg (Image1)

Image1.jpg (Image1)
A table titled 'Susceptibility Test Interpretive Criteria' listing various pathogens and their susceptibility breakpoints. It includes data on disk diffusion zone diameters (in mm) categorized as susceptible, intermediate, or resistant, and minimal inhibitory concentrations (MIC in mcg/mL) with corresponding breakpoints for susceptibility, intermediate, and resistance.*
FDA Label Image

Image2.jpg (Image2)

Image2.jpg (Image2)
A table titled 'Table 2: Acceptable Quality Control Ranges' presenting quality control data for various microorganisms. It lists microorganisms by name and ATCC number, with corresponding disk diffusion zone diameter ranges in mm and minimal inhibitory concentration (MIC) ranges in mcg/mL.*
FDA Label Image

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Image3.jpg (Image3)
A dosage table titled 'Dosage in Neonates (less than or equal to 28 days of postnatal age) for Bacterial Meningitis and Septicemia.' It provides dosing guidelines for different gestational and postnatal age groups, listing specific dosages in mg/kg/day divided by hours.*
FDA Label Image

Image4.jpg (Image4)

Image4.jpg (Image4)
A data table listing NDC numbers, label claims, recommended amounts of diluent, withdrawable volumes, and concentrations for AMPICILLIN SODIUM injection powders. The table shows various strengths ranging from 250 mg to 2 grams, with corresponding diluent volumes and a consistent concentration of 250 mg/mL.*
FDA Label Image

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Image5.jpg (Image5)
A table listing diluents, their concentrations, and stability periods for Ampicillin Sodium injection powder for solution at two storage temperatures: Room Temperature (25°C) and Refrigerated (4°C). It details stability in hours for various diluents such as Sterile Water, Sodium Chloride Injection, Dextrose Injection, and Lactated Ringer's Injection.*
FDA Label Image

Image6.jpg (Image6)

Image6.jpg (Image6)
Table listing NDC numbers, vial descriptions, and package factors for Ampicillin for Injection USP. It includes four vial strengths: 250 mg/10 mL, 500 mg/10 mL, 1 g/15 mL, and 2 g/24 mL, with package counts of either 9 or 10 vials per box.*
FDA Label Image

Image7.jpg (Image7)

Image7.jpg (Image7)
Text panel listing Clinical and Laboratory Standards Institute (CLSI) references for antimicrobial susceptibility testing standards including Performance Standards for Antimicrobial Susceptibility Testing and Disk Diffusion Susceptibility Tests, with specific documents and publication details from 2015.*
FDA Label Image

Label1.jpg (Label1)

Label1.jpg (Label1)
Label for AMPICILLIN 2 g injection powder for solution vial, supplied by Henry Schein, Inc. The label indicates intravenous use with instructions to add sterile water for injection. The vial contains AMPICILLIN SODIUM USP equivalent to 2 g of ampicillin. The label includes storage instructions, manufacturer information, NDC 0404-9818-99, barcode, and placeholders for lot and expiration date.*

* 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.