Lansoprazole Capsule, Delayed Release
Product Images NDC 63629-2341

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 63629-2341). 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 titled 'Mean Severity of Day Heartburn By Study Day For Evaluable Patients' showing severity scores over days from start of treatment. It compares placebo, lansoprazole 15 mg QD, and lansoprazole 30 mg QD, with severity scores on the vertical axis ranging from 0 (None) to 3 (Severe). Severity decreases more in lansoprazole groups compared to placebo over approximately 55 days.*
FDA Label Image

Figure-2.jpg (Figure 2)

Figure-2.jpg (Figure 2)
A line graph titled "Mean Severity of Night Heartburn By Study Day For Evaluable Patients" showing severity levels from 0 (none) to 3 (severe) plotted against days from start of treatment, ranging from -5 to 60. The graph compares placebo, Lansoprazole 15 mg QD, and Lansoprazole 30 mg QD, illustrating a decrease in heartburn severity over time with Lansoprazole treatments having lower severity scores than placebo.*
FDA Label Image

Formula-structure.jpg (Image 01)

Formula-structure.jpg (Image 01)
Chemical structure of lansoprazole, showing its molecular arrangement including a benzimidazole ring bonded to a sulfinyl group and a substituted pyridine ring with trifluoromethoxy and methyl groups.*
FDA Label Image

Label (Lbl636292341)

Label (Lbl636292341)
Label for Lansoprazole Delayed-Release Capsules, USP, 30 mg by Bryant Ranch Prepack. The label includes the NDC 63629-2341-1 with barcode, dosage strength prominently displayed, quantity of 90 capsules, and storage instructions. It states the product is prescription only (Rx only) and includes a note on medication safety and container seal integrity.*

* 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.