Cladribine Injection
Product Images NDC 0143-9871

3 FDA label images from Hikma 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 0143-9871). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma 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.

Product Images & Figures Index

FDA Label Image

Structure (Cladribine Injection Usp 1)

Structure (Cladribine Injection Usp 1)
Chemical structure of cladribine showing a chlorinated purine nucleoside with attached ribose sugar, representing the active ingredient in the Cladribine injection product by Hikma Pharmaceuticals USA Inc.*
FDA Label Image

Cladribine Injection, Usp 10 mg Per 10 mL Container Label (Cladribine Injection Usp 2)

Cladribine Injection, Usp 10 mg Per 10 mL Container Label (Cladribine Injection Usp 2)
Label for Cladribine Injection, USP 10 mg per 10 mL (1 mg/mL) intravenous injection by Hikma Pharmaceuticals USA Inc. The label states the product is a 10 mL single-dose vial that must be diluted prior to intravenous infusion. It includes usage instructions, storage temperature (2° to 8°C), and manufacturer information.*
FDA Label Image

Representative Serialization Image (Cladribine Injection Usp 3)

Representative Serialization Image (Cladribine Injection Usp 3)
A label displaying a data matrix barcode on the left and corresponding text fields on the right. Text includes placeholders for lot number (LOT ABCDE12345), expiration date (EXP MMMYYYY), GTIN (00301234567896), and serial number (SN 12345678901234). No product-specific text or branding is shown.*

* 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.