Ampicillin Injection, Powder, For Solution
Product Images NDC 0781-9409

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ampicillin (NDC 0781-9409). 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.

Product Images & Figures Index

FDA Label Image

Chemical-structure (Ampicillin Pbp Novaplus 01)

Chemical-structure (Ampicillin Pbp Novaplus 01)
This is not-available. This appears to be a chemical formula or code but it does not provide enough context to generate a meaningful description.*
FDA Label Image

Case-label (Ampicillin Pbp Novaplus 02)

Case-label (Ampicillin Pbp Novaplus 02)
Ampicillin for Injection is available in a Pharmacy Bulk Package bottle. It is not intended for direct infusion and must be diluted for intravenous use. Each bottle contains 10 grams of ampicillin sodium. It should be reconstituted with Sterile Water for Injection, USP and further diluted in a suitable fluid. The resulting solution contains 100 mg ampicillin activity per mL. The instructions regarding preparation, dilution, and storage can be found in the insert. The dry powder should be stored between 20°C to 25°C (68°F to 77°F). The product is manufactured in Austria by Sandoz GmbH for Sandoz Inc., Princeton. It is sold in case quantities of 10 Pharmacy Bulk Package Bottles and is for use in a pharmacy admixture service only.*

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