Lansoprazole Capsule, Delayed Release
Product Images NDC 63629-2342

4 FDA label images from Bryant Ranch Prepack · 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 63629-2342). 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)
A line graph showing mean severity of day heartburn over days from start of treatment. The y-axis indicates heartburn severity from 0 (none) to 3 (severe), and the x-axis shows days from -5 to 60. Three lines compare placebo, Lansoprazole 15 mg QD, and Lansoprazole 30 mg QD for evaluable patients.*
FDA Label Image

Figure-2.jpg (Figure 2)

Figure-2.jpg (Figure 2)
A line graph showing mean severity of night heartburn over days from start of treatment. The y-axis measures severity from 0 (none) to 3 (severe). The x-axis measures days from -5 to 60. Three lines represent placebo, lansoprazole 15 mg QD, and lansoprazole 30 mg QD, indicating severity decreases more with lansoprazole, especially at 30 mg.*
FDA Label Image

Formula-structure.jpg (Image 01)

Formula-structure.jpg (Image 01)
Chemical structure of the active ingredient Lansoprazole, shown with its molecular framework including functional groups such as sulfoxide, methyl, pyridine, and trifluoromethoxy substituents.*
FDA Label Image

Label (Lbl636292342)

Label (Lbl636292342)
Lansoprazole Delayed-Release Capsules, USP 30 mg oral capsules, label by Bryant Ranch Prepack. The label includes storage instructions, safety warnings, and a barcode. The package contains 30 capsules and is marked Rx only. The product NDC is 63629-2342-1.*

* 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.