Lansoprazole Capsule, Delayed Release
Product Images NDC 76420-621

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lansoprazole (NDC 76420-621). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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.

FDA Label Image

Lansoprazole-figure-1 (Lansoprazole Figure 1)

A line graph depicting the mean severity of day heartburn by study day for evaluable patients, comparing placebo, Lansoprazole 15 mg once daily (QD), and Lansoprazole 30 mg QD over a period of approximately 60 days from the start of treatment. Severity is rated from 0 (none) to 3 (severe).*

FDA Label Image

Lansoprazole-figure-2 (Lansoprazole Figure 2)

A line graph depicting the mean severity of night heartburn over days from the start of treatment for evaluable patients. The y-axis shows severity levels from 0 (None) to 3 (Severe), and the x-axis shows days from 0 to 60. Three lines represent placebo, Lansoprazole 15 mg QD, and Lansoprazole 30 mg QD, showing trends in symptom severity reduction over time.*

FDA Label Image

Lansoprazole-str (Lansoprazole Str)

Chemical structure of lansoprazole, showing its molecular arrangement including benzene and pyridine rings connected by sulfinyl and methyl groups.*

FDA Label Image

Lansoprazole-label (Lansoprazole Label)

Label for Lansoprazole Delayed-Release Capsules USP 30 mg, quantity 90 capsules. The label indicates relabeling by Enovachem Pharmaceuticals and distribution by Ascend Laboratories, LLC. It includes NDC 76420-621-90, a barcode, QR code, and storage instructions at controlled room temperature (20-25C). The label also references federal dispensing law and prescription status (RX).*

* 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.