Nicardipine Hydrochloride Injection, Solution
Product Images NDC 0517-0735

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 0517-0735). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, Inc., 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

Cardene Structure (Nicardipine Hydrochloride Injection 1)

Chemical structure of nicardipine hydrochloride showing the molecular formula C26H29N3O6·HCl with detailed arrangement of functional groups including nitro, methyl, and ester groups.*

FDA Label Image

Container Label (Nicardipine Hydrochloride Injection 2)

Label for Nicardipine Hydrochloride Injection, USP 2.5 mg/mL (25 mg/10 mL) by American Regent, Inc. The 10 mL single dose vial is for intravenous use only, with a warning to dilute before infusion. Storage instructions are to keep between 20° to 25°C and protect from light. The label includes the NDC 0517-0735-01.*

FDA Label Image

Carton Labeling (Nicardipine Hydrochloride Injection 3)

Package label for Nicardipine Hydrochloride Injection, USP 2.5 mg/mL (25 mg/10 mL) by American Regent, Inc. The label indicates single dose vials with a total of 10 x 10 mL. The product is for intravenous use only and must be diluted before infusion. Storage and composition details are also provided, including the presence of sorbitol and disodium edetate.*

FDA Label Image

Nicardipine Hydrochloride Injection 4

Expiration label for Nicardipine Hydrochloride 2.5 mg/mL Injection, Solution by American Regent, Inc. The label shows a QR code, lot number labeled as TEST, expiration date of 11/2020, GTIN code 00305170735104, and serial number 0.*

* 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.