Nicardipine Hydrochloride Injection, Solution
Product Images NDC 55150-183

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 55150-183). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us 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

Chemical Structure (Nicardipine Str)

Chemical structure of nicardipine hydrochloride showing the molecular arrangement including benzene rings, nitro group, and hydrochloride salt form, consistent with the generic name of the drug.*

FDA Label Image

Nicardipine-fig3 (Nicardipine Fig3)

FDA Label Image

Nicardipine-fig1 (Nicardipine Fig1)

Label for Nicardipine Hydrochloride Injection, USP 25 mg per 10 mL (2.5 mg/mL) sterile single-dose vial. For intravenous infusion only. Distributed by AuroMedics Pharma LLC and made in India. Storage instructions indicate to keep at 20° to 25°C and protect from light. Includes warning that the solution must be diluted before infusion.*

FDA Label Image

Nicardipine-fig2 (Nicardipine Fig2)

Packaging label for Nicardipine Hydrochloride Injection, USP 25 mg/10 mL (2.5 mg/mL) intravenous solution by Eugia US LLC. The label states the product is sterile, for intravenous infusion only, provided as 10 single-dose vials of 10 mL each. Includes a warning that the solution must be diluted before infusion. Distributed by AuroMedics Pharma LLC, made in India. The label features the Novaplus logo and includes storage instructions 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.