Cyclophosphamide
Product Images NDC 72603-326

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Cyclophosphamide (NDC 72603-326). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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 (Cyclophosphamide Injection Usp Aisling 1)

1 (Cyclophosphamide Injection Usp Aisling 1)
Chemical structure of Cyclophosphamide showing a hexagonal ring with a phosphorus-oxygen double bond and an attached N(CH2CH2Cl)2 group plus one water molecule (H2O) indicating the hydrate form.*
FDA Label Image

1 (Cyclophosphamide Injection Usp Aisling 2)

1 (Cyclophosphamide Injection Usp Aisling 2)
Packaging label for Cyclophosphamide for Injection, USP, 500 mg/vial. The label indicates the product is for intravenous infusion or direct injection use as a cytotoxic agent. The labeler is NorthStar Rx LLC, with manufacturing by Amneal Oncology Pvt. Ltd., India. Storage instructions specify keeping the vial at or below 25°C. Additional preparation instructions and regulatory information are also present.*
FDA Label Image

2 (Cyclophosphamide Injection Usp Aisling 3)

2 (Cyclophosphamide Injection Usp Aisling 3)
Cyclophosphamide for Injection, USP 500 mg per vial packaging label from NorthStar Rx LLC. The label indicates it is for intravenous infusion or direct injection use and highlights that the cytotoxic agent must be diluted. It specifies a single-dose vial and includes storage instructions, dosage information, and manufacturer details with a barcode on the side panel.*
FDA Label Image

1 (Cyclophosphamide Injection Usp Aisling 4)

1 (Cyclophosphamide Injection Usp Aisling 4)
Label for Cyclophosphamide for Injection, USP 1 gram/vial, intended for intravenous infusion or direct injection use. It is identified as a cytotoxic agent for single dose use and is sterile and non-pyrogenic. The label includes preparation instructions, storage conditions, manufacturer details, and a barcode. The product is labeled under Northstar Rx LLC.*
FDA Label Image

2 (Cyclophosphamide Injection Usp Aisling 5)

2 (Cyclophosphamide Injection Usp Aisling 5)
Packaging label for Cyclophosphamide for Injection, USP, 1 gram per vial. The label indicates it is a single-dose vial for intravenous infusion or direct injection use and is a cytotoxic agent that must be diluted. The product is manufactured by Amneal Oncology Pvt. Ltd., India, and labeled by NorthStar Rx LLC. The label includes storage instructions and preparation details.*
FDA Label Image

1 (Cyclophosphamide Injection Usp Aisling 6)

1 (Cyclophosphamide Injection Usp Aisling 6)
Label for Cyclophosphamide for Injection, USP 2 gram vial by NorthStar Rx LLC. The label states it is for intravenous infusion or direct injection use, identifies the drug as a cytotoxic agent, single dose, sterile and non-pyrogenic. Preparation instructions for infusion or direct injection and storage conditions are provided. Manufacturer information includes Amneal Oncology Pvt. Ltd., India.*
FDA Label Image

1 (Cyclophosphamide Injection Usp Aisling 7)

1 (Cyclophosphamide Injection Usp Aisling 7)
Cyclophosphamide for Injection, USP 2 gram/vial packaged for intravenous infusion or direct injection use. The label indicates it is a cytotoxic agent that must be diluted and is supplied as a single dose vial. Manufactured for NorthStar Rx LLC and produced by Amneal Oncology Pvt. Ltd. in India, the label includes storage instructions and dilution guidelines.*

* 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.