Cyclophosphamide Injection, Powder, For Solution
Product Images NDC 72572-083

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 72572-083). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Cyclophosphamide Structural Formula (Image 01)

Cyclophosphamide Structural Formula (Image 01)
Chemical structure of cyclophosphamide, displaying molecular bonds including a phosphorus atom bonded to oxygen and nitrogen atoms, alongside other characteristic groups.*
FDA Label Image

Representative Vial Label 72572-085-01 1g (Image 02)

Representative Vial Label 72572-085-01 1g (Image 02)
Label for Cyclophosphamide for Injection, USP, 1 gram per vial. The label states it is a cytotoxic agent for single dose use, sterile, non-pyrogenic, and for parenteral use. Distributed by Civica, Inc. and manufactured by Baxter Healthcare Corporation, made in Germany. Instructions mention use with sterile water for infusion or sodium chloride injection to dissolve the powder.*
FDA Label Image

Representative Carton Label 72572-085-01 1g (Image 03)

Representative Carton Label 72572-085-01 1g (Image 03)
Label for Cyclophosphamide for Injection, USP 1 gram/vial powder for solution, a cytotoxic agent requiring dilution for intravenous or direct injection use. The label shows it is a single-dose vial distributed by Civica, Inc. and manufactured by Baxter Healthcare Corporation, with storage instructions and preparation guidance included.*
FDA Label Image

Representative Vial Label 72572-083-01 2g (Image 04)

Representative Vial Label 72572-083-01 2g (Image 04)
Cyclophosphamide injection powder label showing Cyclophosphamide for Injection, USP with strength of 2 grams per vial. The label states it is a cytotoxic agent for single dose use, sterile, non-pyrogenic, and for parenteral use. The labeler is Civica, Inc., with manufacturing by Baxter Healthcare Corporation. Preparation instructions for intravenous and direct injection are included along with storage conditions.*
FDA Label Image

Representative Carton Label 72572-083-01 2g (Image 05)

Representative Carton Label 72572-083-01 2g (Image 05)
Cyclophosphamide for Injection, USP 2 grams/vial powder for solution packaging label shows a single-dose vial. The label specifies it must be diluted for IV infusion or direct injection use. Distributed by Civica, Inc. and manufactured by Baxter Healthcare Corporation, the label includes dosage preparation instructions and cytotoxic agent warning.*
FDA Label Image

Representative Vial Label 72572-087-01 500 mg (Image 06)

Representative Vial Label 72572-087-01 500 mg (Image 06)
Label for Cyclophosphamide for Injection, USP, 500 mg per vial. The label states it is a cytotoxic agent, for single dose use, sterile and non-pyrogenic for parenteral use. Instructions for dissolving the powder for IV or direct injection are included. The product is distributed by Civica, Inc. and manufactured by Baxter Healthcare Corporation in Germany.*
FDA Label Image

Representative Carton Label 72572-087-01 500 mg (Image 07)

Representative Carton Label 72572-087-01 500 mg (Image 07)
Cyclophosphamide for Injection, USP 500 mg/vial powder for solution carton label by Civica, Inc. The label states the vial is single-dose, must be diluted for intravenous infusion or direct injection. It includes storage instructions, usage dilution directions, and manufacturer details (Baxter Healthcare Corporation). The package displays multiple barcodes and dosage warnings.*

* 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.