Levamlodipine
Product Images NDC 42195-450

3 FDA label images from Xspire Pharma, Llc · 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 Levamlodipine (NDC 42195-450). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xspire Pharma, 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.

FDA Label Image

Chemical Structure (Figure 01)

Chemical Structure (Figure 01)
Chemical structure of Levamlodipine as shown in the image, including its substituted aromatic ring with a chlorine atom, ester groups, and an aminoethoxy side chain, with an additional component indicated by a formula representing malonic acid (C4H4O4).*
FDA Label Image

Principal Display Panel (2.5 mg Tablet Bottle Label)

Principal Display Panel (2.5 mg Tablet Bottle Label)
Levamlodipine Tablets 2.5 mg label shows dosage strength and total count of 30 tablets. The label includes storage instructions, manufacturer information (CSPC Ouyi Pharmaceutical Co., Ltd., China), and distributor details (Xspire Pharma, LLC). It highlights the product is Rx only and features branding logos for CSPC and Xspire Pharma.*
FDA Label Image

Principal Display Panel (5 mg Tablet Bottle Label)

Principal Display Panel (5 mg Tablet Bottle Label)
Levamlodipine Tablets 5 mg label from Xspire Pharma, LLC. The package contains 30 tablets and indicates prescription use (Rx only). Storage instructions specify child-resistant packaging and temperature control from 20°C to 25°C with permitted excursions. Manufactured by CSPC Ouji Pharmaceutical Co., Ltd., China. The label includes barcodes, product codes, and distributor 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.