Kapidex
Product Images NDC 54868-5998

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 Kapidex (NDC 54868-5998). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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.

Product Images & Figures Index

FDA Label Image

Image Of Figure 1: Mean Plasma Graph (Figure 1 Mean Plasma Graph)

Image Of Figure 1: Mean Plasma Graph (Figure 1 Mean Plasma Graph)
A line graph depicting plasma concentration (ng/mL) over time (hours) for Kapidex at two dosages, 30 mg and 60 mg. The graph shows plasma concentration rising and falling for both doses over a 24-hour period, with the 60 mg dose reaching higher concentrations than the 30 mg dose.*
FDA Label Image

Image Of Kapidex Chemical Structure (Kapidex Chemical Structure)

Image Of Kapidex Chemical Structure (Kapidex Chemical Structure)
Chemical structure of dexlansoprazole, the active ingredient in Kapidex, showing the molecular arrangement including the sulfinyl group, pyridine ring with methyl and trifluoroethoxy substituents, and benzimidazole moiety.*
FDA Label Image

Image Of Package Label (Package Label)

Image Of Package Label (Package Label)
Kapidex 30 mg delayed-release capsules packaging label by Physicians Total Care, Inc. The label displays the product name, strength, dosage form (capsules), and quantity (90 capsules). It includes cautionary information about federal law restricting dispensing without prescription and storage instructions. The label also shows the lot number, expiration date, and manufacturer details with barcode.*

* 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.