Cladribine Injection, Solution
Product Images NDC 42658-010

3 FDA label images from Hisun Pharmaceuticals Usa, 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 Cladribine (NDC 42658-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hisun Pharmaceuticals Usa, 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 (Hisun Cladribine 01)

Chemical Structure (Hisun Cladribine 01)
Chemical structure of Cladribine, showing its molecular framework including nitrogen, chlorine, oxygen, and hydrogen atoms. The molecular weight is indicated as 285.7. This represents the active ingredient Cladribine.*
FDA Label Image

Principal Display Panel (10 mL Vial Carton)

Principal Display Panel (10 mL Vial Carton)
Packaging label for Cladribine Injection, USP, 10 mg per 10 mL (1 mg per mL) single dose vial for intravenous infusion. Distributed by Hisun Pharmaceuticals USA, Inc. The label includes storage instructions, lot and expiration information placeholders, ingredient details, and barcodes, with a clear indication that it is Rx only and must be protected from light.*
FDA Label Image

Hisun Cladribine 03

Hisun Cladribine 03
Label for Cladribine Injection, USP, 10 mg per 10 mL (1 mg per mL) intravenous solution. Single dose vial containing 10 mL, distributed by Hisun Pharmaceuticals USA, Inc. The label includes storage instructions to keep refrigerated at 2° to 8°C and protect from light, with directions noted for preparation of intravenous solutions. The product NDC is 42658-010-01.*

* 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.