Ampicillin Powder, For Solution
Product Images NDC 23155-915

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Ampicillin (NDC 23155-915). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals 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

Chemicalstructure (Chemicalstructure)

Chemicalstructure (Chemicalstructure)
Chemical structure diagram showing the molecular composition of Ampicillin, an antibiotic active ingredient used in the product Ampicillin Injection.*
FDA Label Image

Carton-1g (Carton 1g)

Carton-1g (Carton 1g)
Ampicillin for Injection, USP 1 gram per vial powder for solution packaging label. The label indicates the product is for intravenous or intramuscular use and is manufactured by Avet Pharmaceuticals Inc. The carton includes handling instructions, barcode, and storage conditions for the 10 vial package. The product is Rx only.*
FDA Label Image

Carton-250mg (Carton 250mg)

Carton-250mg (Carton 250mg)
Packaging label for Ampicillin for Injection, USP 250 mg* per vial powder for solution by Avet Pharmaceuticals Inc. The label states the product is for intravenous or intramuscular use and includes manufacturer information and storage instructions. The package contains 10 vials of 250 mg each.*
FDA Label Image

Carton-2g (Carton 2g)

Carton-2g (Carton 2g)
Packaging label for Ampicillin for Injection, USP powder for solution, 2 grams per vial, by Avet Pharmaceuticals Inc. The label indicates the drug is for intravenous use only, with each package containing 10 vials of 2 grams each. Manufacturer information and storage instructions are included on the label.*
FDA Label Image

Carton-500mg (Carton 500mg)

Carton-500mg (Carton 500mg)
Packaging label for Ampicillin for Injection, USP, 500 mg per vial, powder for solution. The label indicates the drug is for intravenous or intramuscular use and is manufactured by Avet Pharmaceuticals. The package contains 10 vials of 500 mg each. The label includes storage instructions and a barcode.*
FDA Label Image

Label-1g (Label 1g)

Label-1g (Label 1g)
Ampicillin for Injection, USP 1 gram per vial powder for solution label. It states the product is for intravenous or intramuscular use. The label includes preparation instructions, dosage notes, storage conditions, and manufacturer details for Avet Pharmaceuticals Inc. The label also indicates no varnish on the vial.*
FDA Label Image

Label-250mg (Label 250mg)

Label-250mg (Label 250mg)
Label for Ampicillin for Injection, USP 250 mg per vial, a powder for solution used for intravenous or intramuscular injection. The label includes dosing instructions, storage conditions, and manufacturer information for Avet Pharmaceuticals Inc. The label also features a barcode and is marked as Rx only.*
FDA Label Image

Label-2g (Label 2g)

Label-2g (Label 2g)
Label for Ampicillin for Injection, USP 2 grams per vial, powder for solution for intravenous use. Manufactured for Avet Pharmaceuticals Inc. The label includes dosage preparation instructions, storage conditions, and a barcode. The vial is Rx only and produced by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.*
FDA Label Image

Label-500mg (Label 500mg)

Label-500mg (Label 500mg)
Label for Ampicillin for Injection, USP 500 mg per vial powder for solution by Avet Pharmaceuticals Inc. The vial is for intravenous or intramuscular use, with storage instructions and barcodes visible. The label includes dosage and usage notes and specifies that the product is Rx only.*
FDA Label Image

* 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.