Ampicillin Injection, Powder, For Solution
Product Images NDC 0781-3412

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Ampicillin (NDC 0781-3412). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Chemical-structure (Ampicillin Addv 01)

FDA Label Image

Figure-1-and-figure-2 (Ampicillin Addv 02)

FDA Label Image

Figure-3-and-figure-4 (Ampicillin Addv 03)

FDA Label Image

Figure-5-and-figure-6 (Ampicillin Addv 04)

FDA Label Image

1gm-case-label (Ampicillin Addv 05)

1gm-case-label (Ampicillin Addv 05)
This is a prescription-only medication called Ampicillin for injection, USP, and each vial contains 1 gram of ampicillin sodium. It is intended for intravenous use only and must be used with ADD-Vantage diluent container. The recommended dosage and instructions are found in the accompanying insert. It must be stored at 20° to 25°C (68° to 77°F) and must be used within 1 hour for Dextrose and 6 hours for Sodium Chloride after reconstitution. This medication is manufactured by Sandoz GmbH in Austria for Sandoz Inc. in Princeton, NJ. ADD-Vantage is the trademark of Hospira, Inc.*
FDA Label Image

2-grams-case-label (Ampicillin Addv 06)

2-grams-case-label (Ampicillin Addv 06)
This is a medication called Ampicillin for Injection, USP. It is available in a package consisting of 10 single-dose vials, each containing 2 grams of ampicillin. The medication is intended for intravenous use only and is to be used with the ADD-Vantage diluent container. The medication should be stored at a temperature of 20° to 25°C and after reconstitution, it should be used within 1 hour for Dextrose and 6 hours for Sodium Chloride. The medication is manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540. Usual Dosage information can be found in the accompanying insert.*

* 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.