Nicardipine Hydrochloride Injection, Solution
Product Images NDC 71288-204

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 71288-204). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal Pharmaceuticals 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

Principal Display Panel – Nicardipine Hydrochloride Injection, Usp 10 mL Carton (Nicard Carton V3)

Principal Display Panel – Nicardipine Hydrochloride Injection, Usp 10 mL Carton (Nicard Carton V3)
Flattened carton packaging for nicardipine hydrochloride injection USP, 2.5 mg/mL, by Meitheal Pharmaceuticals Inc. The label indicates a 10 x 10 mL single-dose vial carton with a dosage strength of 25 mg per 10 mL. The carton includes usage instructions emphasizing dilution before infusion and storage conditions at controlled room temperature.*
FDA Label Image

Structure (Nicard Structure)

Structure (Nicard Structure)
Chemical structure of nicardipine hydrochloride shown as a 2D molecular diagram with attached hydrochloride group.*
FDA Label Image

Principal Display Panel – Nicardipine Hydrochloride Injection, Usp 10 mL Vial Label (Nicard Vial V3)

Principal Display Panel – Nicardipine Hydrochloride Injection, Usp 10 mL Vial Label (Nicard Vial V3)
Label for nicardipine hydrochloride injection, USP, 25 mg per 10 mL (2.5 mg per mL) solution for intravenous use. It is a single-dose vial containing 10 mL. The label indicates it is Rx only and must be diluted before infusion. Manufactured by Meitheal Pharmaceuticals Inc., Chicago, IL, with manufacturing in China.*

* 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.