Lansoprazole Capsule, Delayed Release
Product Images NDC 63629-2340

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lansoprazole (NDC 63629-2340). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Figure-1.jpg (Figure 1)

Figure-1.jpg (Figure 1)
This is a chart that shows the mean severity of day heartburn by study day for evaluable patients. The severity is measured on a scale of 0 (none) to 3 (severe). The chart includes data for a placebo group and two groups taking different doses of lansoprazole. The chart is broken down by the number of days from the start of treatment.*
FDA Label Image

Figure-2.jpg (Figure 2)

Figure-2.jpg (Figure 2)
The text represents a table that shows the Mean Severity of Night Heartburn for different treatment groups (Placebo, Lansoprazole 15mg QD, and Lansoprazole 30mg QD) on different study days. The severity is measured on a scale of 0 to 3, where 0 means no heartburn and 3 means severe heartburn. The table also shows the percentage of patients who experienced heartburn on each study day.*
FDA Label Image

Formula-structure.jpg (Image 01)

Formula-structure.jpg (Image 01)
FDA Label Image

Label (Lbl636292340)

Label (Lbl636292340)
This text is a product label for Lansoprazole Delayed-Release Capsules, 30 mg manufactured by BRP Pharmaceuticals. It also contains instructions for storage and dispensing.*

* 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.