Amiodarone Hydrochloride Tablet
Product Images NDC 70518-1939

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Amiodarone Hydrochloride (NDC 70518-1939). 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 200mg 70518 1939 01

Amiodarone HCl 200mg 70518 1939 01
Amiodarone HCI is a prescription-only medication manufactured by Aurobindo in India. It is packaged with an NDC number and lot number. The medication should be kept out of the reach of children, and the packaging includes a package insert with instructions for use. It should be stored at a temperature between 20-26°C (63-77°F), with excursions permitted up to 15-30°C (59-86°F) as per USP regulations. The medication has been repackaged by RemedyRepack Inc. in Indiana, PA with their phone number included.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Amiodarone HCI is a medication that is available through prescription only. The medication is packaged with an NDC number, a lot number, and an expiration date. The medication is manufactured by Aurcbindo in India and should be kept out of the reach of children. The directions for use are located in the package insert. The medication should be stored between 20-26°C but may be stored at 15-30°C with excursions permitted as outlined by USP. The medication was repackaged by RemedyRepack Inc. and contact information is provided.*
FDA Label Image

Chemical Structure (Amiodarone Str)

* 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.