Amiodarone Hydrochloride Injection, Solution
Product Images NDC 65219-645

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Amiodarone Hydrochloride (NDC 65219-645). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structural Formula (Ami0c 0001 01)

Chemical structure of amiodarone hydrochloride showing its molecular composition with iodine atoms, aromatic rings, and a hydrochloride group.*

FDA Label Image

Fresenius Kabi Logo (Ami0c 0001 02)

FDA Label Image

Amiod-label-01.jpg (Amiod Label 01)

Label for Amiodarone Hydrochloride Injection, USP 150 mg per 3 mL (50 mg per mL) intravenous solution. The label indicates it is a single dose vial of 3 mL, requiring dilution before IV use. The product is manufactured by Fresenius Kabi USA, LLC, Lake Zurich, IL. Additional information includes storage instructions and a barcode.*

FDA Label Image

Amiod-label-02.jpg (Amiod Label 02)

Label for Amiodarone Hydrochloride Injection, USP 150 mg per 3 mL (50 mg per mL) intravenous solution. The package contains 25 single-dose vials of 3 mL each. Labeler is Fresenius Kabi USA, LLC. The label includes dilution instructions, storage conditions, and a barcode with NDC number 65219-643-03.*

FDA Label Image

Amiod-label-03.jpg (Amiod Label 03)

Label for Amiodarone Hydrochloride Injection, USP 50 mg/mL, packaged as 450 mg per 9 mL in a single-dose vial. The label indicates the product is for intravenous use only, requires dilution, and is sterile. It is manufactured by Fresenius Kabi USA, LLC, Lake Zurich, Illinois.*

FDA Label Image

Amiod-label-04.jpg (Amiod Label 04)

Label for Amiodarone Hydrochloride Injection, USP 50 mg/mL, presented as 450 mg per 9 mL. It is for intravenous use only and must be diluted before administration. The package contains 10 single-dose vials, labeled as Sterile and Rx only. The label warns to protect from light and excessive heat, storing between 20° to 25°C, and notes the container closure is not made with natural rubber latex. The label includes manufacturer information for Fresenius Kabi USA, LLC.*

* 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.