Amiodarone Hydrochloride Injection, Solution
Product Images NDC 70436-232

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Amiodarone Hydrochloride (NDC 70436-232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Slate Run Pharmaceuticals, 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 of amiodarone hydrochloride, showing the arrangement of atoms and bonds including iodine atoms, methyl groups, and an ethylamine side chain with hydrochloride form, consistent with the active ingredient in Amiodarone Hydrochloride injection.*

FDA Label Image

70436-232-72 (Image 1)

Amiodarone Hydrochloride Injection, USP 150 mg/3 mL (50 mg/mL) intravenous solution in a 3 mL single-dose vial. The label indicates the product must be diluted before intravenous use and is manufactured by Zhejiang Poly Pharm. Co., Ltd., distributed by Slate Run Pharmaceuticals. The label includes storage instructions, barcode, lot, and expiration details.*

FDA Label Image

70436-232-73 (Image 2)

Label for Amiodarone Hydrochloride Injection, USP 450 mg/9 mL (50 mg/mL) single-dose vial by Slate Run Pharmaceuticals. The label includes dosage information, storage instructions, and warnings for intravenous use only, dilution requirements, and light protection. NDC 70436-232-73 is shown along with manufacturer details and a barcode.*

FDA Label Image

70436-232-74 (Image 3)

Label for Amiodarone Hydrochloride Injection, USP, 50 mg/mL (900 mg/18 mL) single-dose vial by Slate Run Pharmaceuticals. The label includes dosage instructions, storage conditions (20° to 25°C), warnings to protect from light and excessive heat, and manufacturing details from Zhejiang Poly Pharm. Co., Ltd. It also presents an NDC code (70436-232-74) and a barcode.*

* 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.