Nicardipine Hydrochloride Injection
Product Images NDC 82432-103

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 Nicardipine Hydrochloride (NDC 82432-103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chengdu Shuode Pharmaceutical Co., Ltd, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Structure (1)

Structure (1)
Chemical structure of Nicardipine Hydrochloride, showing the molecular formula C26H29N3O6·HCl with labeled atoms and bonds in the compound's two-dimensional structure.*
FDA Label Image

Vial Label (2)

Vial Label (2)
Label for Nicardipine Hydrochloride Injection, 25 mg/10 mL (2.5 mg/mL) in a 10 mL single dose vial. It is for intravenous use only and must be diluted before infusion. The label states the product contains nicardipine hydrochloride, benzoic acid, sodium chloride in water for injection, and sodium hydroxide. Manufactured by Chengdu Shuode Pharmaceutical Co., Ltd.*
FDA Label Image

Carton Label (3)

Carton Label (3)
Packaging label for Nicardipine Hydrochloride Injection 25 mg/10 mL (2.5 mg/mL) single-dose vial, for intravenous use. The label includes warnings to dilute before infusion and discard unused portion, storage conditions, and manufacturer details: Chengdu Shuode Pharmaceutical Co., Ltd, Chengdu, Sichuan, China. The label also features a barcode and a 2D data matrix code with tamper-evident information.*

* 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.