Penicillin G Potassium Injection, Powder, For Solution
Product Images NDC 0781-6136

3 FDA label images from Sandoz Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Penicillin G Potassium (NDC 0781-6136). 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 (Penicillin Potassium 01)

Chemical-structure (Penicillin Potassium 01)
Chemical structure of Penicillin G Potassium, illustrating its characteristic beta-lactam ring alongside the phenylacetyl side chain and potassium salt form.*
FDA Label Image

5-million-case-label (Penicillin Potassium 02)

5-million-case-label (Penicillin Potassium 02)
Label for Penicillin G Potassium for Injection, USP, 5,000,000 units (5 million units) powder for solution, for intramuscular or intravenous use. The package contains 10 vials, labeled by Sandoz Inc. The label includes preparation instructions for solution concentrations with varying diluent amounts and storage conditions for the dry powder and constituted solution.*
FDA Label Image

20-million-carton (Penicillin Potassium 03)

20-million-carton (Penicillin Potassium 03)
Packaging label for Buffered Penicillin G Potassium for Injection, USP 20,000,000 units (20 million units) in powder form for solution. The label indicates it is for IV use, contains 1 vial per package, and is manufactured by Sandoz Inc. The label includes preparation instructions, storage conditions, and a barcode.*

* 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.