Lansoprazole Capsule, Delayed Release
Product Images NDC 82461-713

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lansoprazole (NDC 82461-713). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medcore 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

Lansoprazole-figure-1 (Lansoprazole Figure 1)

A line graph showing the mean severity of day heartburn over days from the start of treatment for evaluable patients. The severity scale ranges from 0 (none) to 3 (severe). Three groups are compared: placebo, lansoprazole 15 mg QD, and lansoprazole 30 mg QD, with lansoprazole groups showing lower mean severity over time compared to placebo.*

FDA Label Image

Lansoprazole-figure-2 (Lansoprazole Figure 2)

A line graph showing mean severity of night heartburn over days from start of treatment among evaluable patients. The y-axis measures mean severity from 0 (none) to 3 (severe), and the x-axis shows days from 0 to 60. Three lines compare placebo, Lansoprazole 15 mg once daily, and Lansoprazole 30 mg once daily, illustrating changes in symptom severity over time.*

FDA Label Image

Lansoprazole-str (Lansoprazole Str)

Chemical structure diagram of lansoprazole, showing the molecular arrangement of its atoms and functional groups.*

FDA Label Image

Lansoprazole-30mg-30s-b (Lansoprazole 30mg 30s B)

Label of Lansoprazole delayed-release capsules, 30 mg, by Medcore LLC. The label states each pink and black capsule contains Lansoprazole USP and is imprinted with '263'. The package contains 30 capsules and includes storage instructions, dosage notes, and distributor information, including a barcode and QR code.*

* 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.