Amiodarone Hydrochloride Injection, Solution
Product Images NDC 72673-073

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amiodarone Hydrochloride (NDC 72673-073). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zhejiang Poly Pharm. Co., Ltd., 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

Amiodarone Structural Formula (Image 02)

Chemical structure diagram of amiodarone hydrochloride, showing its molecular framework with iodine atoms, ether and amine groups, and associated hydrochloride.*

FDA Label Image

Amiodarone Hydrochloride Injection Usp, 150 mg/3 mL Carton Label (Image 1)

Amiodarone Hydrochloride Injection, USP 150 mg/3 mL (50 mg/mL) single-dose vials for intravenous use only. The label indicates the product must be diluted before use. The package contains 10 single-dose 3 mL vials. Manufactured by Zhejiang Poly Pharm. Co., Ltd. in China and labeled by Hainan Poly Pharm. Co., Ltd.*

FDA Label Image

Amiodarone Hydrochloride Injection Usp, 450 mg/9 mL Carton Label (Image 2)

Packaging label for Amiodarone Hydrochloride Injection, USP, 450 mg/9 mL (50 mg/mL) intravenous solution. The label indicates single-dose vials, 10 x 9 mL, for intravenous use only. It states the product must be diluted and is for prescription use only. Manufactured by Zhejiang Poly Pharm. Co., Ltd., China, with additional manufacturing by Hainan Poly Pharm. Co., Ltd. Ingredients and handling instructions are also shown, alongside a barcode.*

FDA Label Image

Amiodarone Hydrochloride Injection Usp, 900 mg/18 mL Carton Label (Image 3)

Packaging label for Amiodarone Hydrochloride Injection, USP 900 mg/18 mL (50 mg/mL) intravenous solution. The label states it must be diluted and is for single-dose vial use only. Manufactured by Zhejiang Poly Pharm. Co., Ltd. and labeled for Haian Poly Pharm. Co., Ltd. Includes storage and handling instructions, active ingredients per mL, and barcode. The label features the Poly Pharm logo.*

* 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.