Nicardipine Hydrochloride Injection
Product Images NDC 82432-103

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.

FDA Label Image

Structure (1)

FDA Label Image

Vial Label (2)

This is a description of Nicardipine Hydrochloride Injection, a medication used for intravenous use to treat certain heart conditions. The prescription drug comes in a 25 mg/10 mL strength, with each vial containing 25 mg nicardipine hydrochloride. It is important to dilute the solution before infusion and discard any unused portion. The medication also contains benzoic acid and sodium chloride in Water for Injection. The pH is adjusted to 3.2 - 4.2, and it should be protected from light and stored at 20°C to 25°C. The manufacturer is Chengdu Shuode Pharmaceutical Co., Ltd.*

FDA Label Image

Carton Label (3)

This is a pharmaceutical product label for Nicardipine Hydrochloride Injection, emphasizing the need to dilute before infusion and discard unused portions. The product contains Nicardipine hydrochloride, Baracicacia, and Sodium Chloride for intravenous use only. It warns against the presence of particulate matter and advises storage at controlled room temperature away from light. The manufacturer is Chengdu Shuod Pharmaceutical Co., Ltd based in Sichuan, China.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.