Cyclophosphamide
Product Images NDC 81298-8112

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Cyclophosphamide (NDC 81298-8112). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Long Grove 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

Cyclophosphamide Structural Formula (Cyclophosphamide Injection Powder For Solution 1)

Chemical structure diagram of cyclophosphamide monohydrate showing a phosphoramide group attached to a hexagonal ring, including oxygen, nitrogen atoms, and two chloroethyl side chains.*

FDA Label Image

Cyclophosphamide For Injection, 500mg Vial Label (Cyclophosphamide Injection Powder For Solution 2)

This is a drug facts label for Cyclophosphamide for Injection, USP 500 mg/vial. It is indicated for intravenous infusion or direct injection use and is a cytotoxic agent. The label includes instructions for dilution and storage, a warning that it is sterile, non-pyrogenic, and states that it is manufactured for Long Grove Pharmaceuticals, LLC.*

FDA Label Image

Cyclophosphamide For Injection 500mg Carton Label (Cyclophosphamide Injection Powder For Solution 3)

Carton label for Cyclophosphamide for Injection, USP 500 mg/vial by Long Grove Pharmaceuticals, LLC. The label includes dilution instructions for intravenous infusion or direct injection and warnings about cytotoxicity. It also shows the NDC number 81298-8110-1, storage instructions, and manufacturer details including manufacturing location in Taiwan.*

FDA Label Image

Cyclophosphamide For Injection, Usp 1g Vial Label (Cyclophosphamide Injection Powder For Solution 4)

Label for Cyclophosphamide for Injection, USP 1 gram/vial by Long Grove Pharmaceuticals, LLC. The label states it is for intravenous infusion or direct injection use and is a cytotoxic agent in a single-dose vial. Storage instructions and preparation details for infusion and injection use are included. Manufactured in Taiwan.*

FDA Label Image

Cyclophosphamide For Injection, Usp 1g Carton Label (Cyclophosphamide Injection Powder For Solution 5)

Packaging label for Cyclophosphamide for Injection, USP, 1 gram per vial, by Long Grove Pharmaceuticals, LLC. The label shows the NDC 81298-8112-1 and states the product is for intravenous infusion or direct injection use and is a cytotoxic agent. Storage instructions and dilution preparation details are included. The label also displays the Long Grove Pharmaceuticals logo and a barcode, with manufacturing information indicating production in Taiwan.*

FDA Label Image

Cyclophosphamide For Injection, Usp 2g Vial Label (Cyclophosphamide Injection Powder For Solution 6)

Label for Cyclophosphamide for Injection, USP 2 gram/vial by Long Grove Pharmaceuticals, LLC. The vial is single-dose, intended for intravenous infusion or direct injection use as a cytotoxic agent. The label includes dosage preparation instructions, storage conditions (at or below 25°C), and manufacturing information.*

FDA Label Image

Cyclophosphamide For Injection, Usp 2g Carton Label (Cyclophosphamide Injection Powder For Solution 7)

Cyclophosphamide for Injection, USP 2 gram/vial packaging label from Long Grove Pharmaceuticals, LLC. The label states the product is a cytotoxic agent for intravenous infusion or direct injection use, must be diluted, and contains 2 grams of cyclophosphamide per vial. It includes storage instructions, NDC 81298-8114-1, and identifies the product as sterile, non-pyrogenic. The product is manufactured in Taiwan for Long Grove Pharmaceuticals, Rosemont, IL.*

* 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.