Nicar-img-01.jpg (Nicar Img 01)
Nicardipine Hydrochloride Injection
Product Images NDC 65219-298
10 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Nicardipine Hydrochloride (NDC 65219-298). 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.
Product Images & Figures Index
Nicar-label-01.jpg (Nicar Label 01)
Label for Nicardipine Hydrochloride Injection 0.1 mg/mL (20 mg in 200 mL) in 0.9% Sodium Chloride for intravenous infusion. The label includes dosing caution, storage instructions (20° to 25°C, protect from light), and notes it is a single dose 200 mL iso-osmotic container. Manufactured for Fresenius Kabi USA, LLC, made in Italy.*
Nicar-label-02.jpg (Nicar Label 02)
Label for Nicardipine Hydrochloride Injection, 0.1 mg/mL, in a 200 mL single dose container for intravenous infusion. It contains 20 mg per container (0.1 mg/mL). The label includes usage cautions, storage instructions, and manufacturer information from Fresenius Kabi USA, LLC. The solution is sterile, nonpyrogenic, and in 0.9% sodium chloride injection.*
Nicar-label-03.jpg (Nicar Label 03)
Label for Nicardipine Hydrochloride Injection 0.1 mg/mL in 0.9% Sodium Chloride Injection, strength 20 mg in 200 mL. The label indicates it is for intravenous infusion and is Rx only. The labeler is Fresenius Kabi USA, LLC.*
Nicar-label-04.jpg (Nicar Label 04)
Label for Nicardipine Hydrochloride 0.1 mg/mL Injection in 0.9% Sodium Chloride, 20 mg in 200 mL. The product is packaged as 10 single-dose containers of 200 mL each. Manufactured for Fresenius Kabi USA, LLC, Lake Zurich, IL, made in Italy. The label includes storage instructions, expiration date, lot number, and barcodes.*
Nicar-label-05.jpg (Nicar Label 05)
Label of Nicardipine Hydrochloride injection in a 0.2 mg/mL strength, equivalent to 40 mg in 200 mL 0.9% Sodium Chloride Injection. The product is for intravenous infusion, sterile and nonpyrogenic. It is manufactured for Fresenius Kabi USA, LLC, and made in Italy. The label includes storage instructions, cautions, and dosage guidance references.*
Nicar-label-06.jpg (Nicar Label 06)
Label for Nicardipine Hydrochloride injection, 0.2 mg/mL concentration, with a total of 40 mg in 200 mL volume. The label indicates it is for intravenous infusion in 0.9% Sodium Chloride Injection, manufactured by Fresenius Kabi USA, LLC. The label includes warnings such as checking infusion rate for double concentration, storage instructions between 20° to 25°C, and cautions against use of non-clear solutions or supplemental medication.*
Nicar-label-07.jpg (Nicar Label 07)
Nicardipine Hydrochloride 0.2 mg/mL injection in 0.9% Sodium Chloride, 40 mg in 200 mL intravenous infusion. The label is for an intravenous use solution by Fresenius Kabi USA, LLC, including the NDC 65219-298-01 and Rx only status.*
Nicar-label-08.jpg (Nicar Label 08)
Label for Nicardipine Hydrochloride injection in 0.9% Sodium Chloride, 0.2 mg/mL (40 mg in 200 mL). Packaging includes 10 single-dose containers of 200 mL each. Manufactured for Fresenius Kabi USA, LLC, made in Italy. Storage instructions specify 20 to 25°C (68 to 77°F) and protection from light and excessive heat. The label features NDC 65219-298-20 with lot number, expiration date, and barcodes.*
Nicar-struc-01.jpg (Nicar Struc 01)
Chemical structure of Nicardipine Hydrochloride. The diagram shows the molecular structure with labeled rings, functional groups, and atoms representing the compound's chemical composition.*
* 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.
