Clofarabine Injection
Product Images NDC 70121-1236

3 FDA label images from Amneal Pharmaceuticals Llc · 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 Clofarabine (NDC 70121-1236). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

1 (Clofarabine Injection 1)

1 (Clofarabine Injection 1)
Chemical structure of the active ingredient Clofarabine, showing its molecular framework with nitrogen, oxygen, fluorine, chlorine atoms, and hydroxyl groups in the structure.*
FDA Label Image

1 (Clofarabine Injection 2)

1 (Clofarabine Injection 2)
Clofarabine Injection 20 mg/20 mL (1 mg/mL) single-dose vial label by Amneal Pharmaceuticals LLC. Label includes storage instructions, dilution requirement prior to intravenous use, and manufacturer details for Amneal Oncology Pvt. Ltd., India. Barcode and lot information area also visible.*
FDA Label Image

2 (Clofarabine Injection 3)

2 (Clofarabine Injection 3)
Label for Clofarabine Injection 20 mg/20 mL (1 mg/mL) single-dose vial by Amneal Pharmaceuticals LLC. The label states the product must be diluted prior to intravenous use, with storage instructions (20° to 25°C), and notes sterile, preservative-free formulation. Manufactured by Amneal Oncology Pvt. Ltd., India, distributed by Amneal Pharmaceuticals in New Jersey.*

* 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.