Cupric Chloride Injection, Solution
Product Images NDC 80830-2301

View Photos of 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 Cupric Chloride (NDC 80830-2301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Private Limited, 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

1 (Cupric Chloride Injection Usp 1)

1 (Cupric Chloride Injection Usp 1)
Chemical structure of cupric chloride dihydrate showing copper (Cu) bonded to two chlorine (Cl) atoms and two water molecules (H2O).*
FDA Label Image

2 (Cupric Chloride Injection Usp 2)

2 (Cupric Chloride Injection Usp 2)
Label for Cupric Chloride Injection, USP 4 mg/10 mL (0.4 mg/mL) intravenous solution. The label states it is for intravenous use only after dilution and to discard unused portion. It is a 10 mL single-dose vial distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ, and made in India. The label includes a barcode and mentions the product's pH adjustment and ingredient details.*
FDA Label Image

1 (Cupric Chloride Injection Usp 3)

1 (Cupric Chloride Injection Usp 3)
Packaging label for Cupric Chloride Injection, USP 4 mg/10 mL (0.4 mg/mL) intravenous solution by Amneal Pharmaceuticals, showing product name, strength, dosage form, caution for intravenous use only after dilution, and manufacturer and distributor information. The package contains 25 single-dose 10 mL vials. Storage and handling instructions are included.*

* 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.