Cupric Chloride Injection, Solution
Product Images NDC 51754-0103

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Cupric Chloride (NDC 51754-0103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Exela Pharma Sciences, Llc, 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

Logo (Image 01)

FDA Label Image

Vial Label (Image 02)

Vial Label (Image 02)
Label for Cupric Chloride Injection, USP 0.4 mg/mL (4 mg/10 mL), an injectable solution for intravenous use. The label states Rx Only, NDC 51754-0103-1, and indicates it is a 10 mL single-dose vial. Manufacturer is Exela Pharma Sciences, LLC. The label includes dilution instructions and warnings to discard unused portions.*
FDA Label Image

10 Ct Carton (Image 03)

10 Ct Carton (Image 03)
Packaging label for Cupric Chloride Injection, USP 4 mg/10 mL (0.4 mg/mL) intravenous injection, solution. The label indicates it is for Rx only, with a caution for intravenous use only after dilution. The product is supplied as 10 single-dose vials, 10 mL each. Labeler is Exela Pharma Sciences, LLC, made in the USA.*
FDA Label Image

25 Ct Carton (Image 04)

25 Ct Carton (Image 04)
Packaging label for Cupric Chloride Injection, USP 4 mg/10 mL (0.4 mg/mL) single-dose vials by Exela Pharma Sciences, LLC. The label indicates the injection is for intravenous use only after dilution, supplied in a 25 x 10 mL vial carton. Storage conditions and cautionary statements 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.