Amiodarone Hydrochloride Injection, Solution
Product Images NDC 55150-182

7 FDA label images from Auromedics Pharma Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Amiodarone Hydrochloride (NDC 55150-182). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Auromedics Pharma 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

Package Label-principal Display Panel (150 mg per 3 mL (50 mg / mL) Container Label)

Package Label-principal Display Panel (150 mg per 3 mL (50 mg / mL) Container Label)
Label for Amiodarone Hydrochloride Injection, USP 150 mg per 3 mL (50 mg/mL) intravenous solution by AuroMedics Pharma LLC. The label states 'For I.V. Use Only' and 'MUST BE DILUTED'. It is a sterile, single-dose 3 mL vial. The label includes product ingredients and manufacturer information.*
FDA Label Image

Package Label-principal Display Panel (150 mg per 3 mL (50 mg / mL) Container-Carton (10 Vials))

Package Label-principal Display Panel (150 mg per 3 mL (50 mg / mL) Container-Carton (10 Vials))
Packaging label for Amiodarone Hydrochloride Injection, USP, 150 mg per 3 mL (50 mg/mL) intravenous injection solution. Box contains 10 single-dose vials of 3 mL each. Label indicates the product must be diluted before use. Distributed by AuroMedics Pharma LLC, the label includes storage instructions and a barcode.*
FDA Label Image

Package Label-principal Display Panel (450 mg per 9 mL (50 mg / mL) Container Label)

Package Label-principal Display Panel (450 mg per 9 mL (50 mg / mL) Container Label)
Amiodarone Hydrochloride Injection, USP 450 mg per 9 mL (50 mg/mL) in a single dose 9 mL vial. Label indicates intravenous use only, must be diluted, sterile product, distributed by AuroMedics Pharma LLC. Includes dosage information and storage instructions, with a barcode and QR code visible.*
FDA Label Image

Package Label-principal Display Panel (450 mg per 9 mL (50 mg / mL) Container-Carton (10 Vials))

Package Label-principal Display Panel (450 mg per 9 mL (50 mg / mL) Container-Carton (10 Vials))
Packaging label for Amiodarone Hydrochloride Injection, USP, 450 mg per 9 mL (50 mg/mL) intravenous injection solution. The label indicates single dose vials, 10 vials of 9 mL each, must be diluted before use, and is distributed by AuroMedics Pharma LLC. The label includes storage instructions and a barcode.*
FDA Label Image

Package Label-principal Display Panel (900 mg per 18 mL (50 mg / mL) Container Label)

Package Label-principal Display Panel (900 mg per 18 mL (50 mg / mL) Container Label)
Label for Amiodarone Hydrochloride Injection, USP 900 mg per 18 mL (50 mg/mL) intravenous solution. The 18 mL multiple dose vial is sterile and must be diluted before use. Labeled for prescription use only. Distributed by AuroMedics Pharma LLC, made in India. Includes storage instructions and ingredient details.*
FDA Label Image

Package Label-principal Display Panel (900 mg per 18 mL (50 mg / mL) Container-Carton (1 Vial))

Package Label-principal Display Panel (900 mg per 18 mL (50 mg / mL) Container-Carton (1 Vial))
Packaging label for Amiodarone Hydrochloride Injection, USP 900 mg per 18 mL (50 mg/mL) sterile intravenous injection solution. The label states it is a multiple-dose vial containing 18 mL and must be diluted before use. Distributed by AuroMedics Pharma LLC.*
FDA Label Image

Amiodarone Hydrochloride Chemical Structure (Amiodarone Str)

Amiodarone Hydrochloride Chemical Structure (Amiodarone Str)
Chemical structure diagram of amiodarone hydrochloride, showing its molecular framework with various ring systems and substituents as depicted in black line drawing.*

* 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.