Amiodarone Hydrochloride Injection, Solution
Product Images NDC 70518-1231

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amiodarone Hydrochloride (NDC 70518-1231). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Amiodarone HCl 150mg 3ml (50mg mL) 70518 1231 00

Label for Amiodarone Hydrochloride injection solution, 150 mg/3 mL (50 mg/mL) strength. The label indicates it is for intravenous use only and contains 3 single-dose vials. The product is repackaged by RemedyRepack Inc. and manufactured by West-Ward Pharma in EatonTown, NJ. The label includes a warning that the solution must be diluted before use and storage instructions at 20-25°C with permitted excursions.*

FDA Label Image

Amiodarone HCl 150mg 3ml (50mg mL) 70518 1231 01

Label for Amiodarone Hydrochloride injection, 50 mg/mL strength in a 3 mL vial, with a total of 150 mg per vial. The label states it is for intravenous use, single dose vials, quantity of 25. Repackaged by RemedyRepack Inc. The label includes warnings such as 'Must Be Diluted' and storage instructions. Manufacturer is West-Ward Pharma, Eatontown, NJ.*

FDA Label Image

Chemical Structure (Amiodarone HCl Injection 1)

Chemical structure of Amiodarone Hydrochloride, illustrating its molecular configuration with iodine atoms, aromatic rings, and associative functional groups, consistent with its chemical identity.*

* 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.