Lansoprazole Capsule, Delayed Release
Product Images NDC 72162-1976

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 72162-1976). 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 the mean severity of day heartburn by study day for evaluable patients. The y-axis measures mean severity of day heartburn from 0 (none) to 3 (severe), and the x-axis represents days from the start of treatment, ranging from -5 to 60. The graph compares placebo, lansoprazole 15 mg once daily, and lansoprazole 30 mg once daily, with both doses showing reduced heartburn severity over time compared to placebo.*
FDA Label Image

Figure-2.jpg (Figure 2)

Figure-2.jpg (Figure 2)
A line graph depicting the mean severity of night heartburn over days from the start of treatment for evaluable patients, comparing placebo, Lansoprazole 15 mg QD, and Lansoprazole 30 mg QD. The y-axis shows mean severity from 0 (none) to 3 (severe), and the x-axis shows days from -5 to 60.*
FDA Label Image

Formula-structure.jpg (Image 01)

Formula-structure.jpg (Image 01)
Chemical structure of lansoprazole showing its molecular composition including benzazole, sulfoxide, methyl, and trifluoromethoxy functional groups.*
FDA Label Image

Label (Lbl721621976)

Label (Lbl721621976)
Lansoprazole Delayed-Release Capsules, USP 30 mg, in a label showing a package of 30 capsules. The label includes the NDC 72162-1976 and indicates the product is Rx only. It is relabeled by Bryant Ranch Prepack and manufactured by Laboratorios Liconsa SAU. The label also provides storage instructions and a medication guide website link.*

* 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.