Nicardipine Hydrochloride Injection
Product Images NDC 65219-818

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 65219-818). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structure (Nic02 0000 01)

Structure (Nic02 0000 01)
Chemical structure diagram of Nicardipine Hydrochloride showing its molecular framework including aromatic rings, nitro, methoxy, methyl, and hydrochloride components.*
FDA Label Image

Fresenius Kabi Logo (Nic02 0000 02)

FDA Label Image

Principal Display Panel – Vial Label (Nic02 0000 03)

Principal Display Panel – Vial Label (Nic02 0000 03)
Label for Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) intravenous injection by Fresenius Kabi USA, LLC. The label indicates it is a 10 mL single dose vial, with warnings to dilute before infusion, discard unused portion, and use for intravenous administration only. Storage instructions are 20° to 25°C, with product manufactured in China. Includes NDC 65219-818 and barcode.*
FDA Label Image

Principal Display Panel – Individual Carton (Nic02 0000 04)

Principal Display Panel – Individual Carton (Nic02 0000 04)
Packaging label for NICARDIPINE HYDROCHLORIDE 25 mg/10 mL (2.5 mg/mL) Hydrochloride Injection by Fresenius Kabi USA, LLC. The label indicates the drug is for intravenous use only, supplied as a single 10 mL vial. Storage instructions and a barcode are also visible, along with warnings to dilute before infusion and to discard unused portions.*

* 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.