Omeprazole Capsule, Delayed Release
Product Images NDC 62175-136

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 62175-136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Chemical Structure (Omeprazole Delayed Release Capsules 1)

Chemical structure of omeprazole, the active ingredient in Omeprazole delayed-release capsules from Lannett Company, Inc.*

FDA Label Image

Label (Omeprazole Delayed Release Capsules 2)

Label for Omeprazole Delayed-Release Capsules, USP, 10 mg strength in a 30-capsule package. The label includes storage instructions to keep the capsules protected from light and moisture at controlled room temperature. Distributed by Lannett Company, Inc., Philadelphia, PA. Features a barcode and a note directing to Lannett's website for medication guides.*

FDA Label Image

Label (Omeprazole Delayed Release Capsules 3)

Label for Omeprazole Delayed-Release Capsules, USP 20 mg by Lannett Company, Inc. The label specifies storage instructions, dosage form as delayed-release capsules, and indicates that the product is prescription only with a package size of 30 capsules. The label also features a barcode and the Lannett logo.*

FDA Label Image

Label (Omeprazole Delayed Release Capsules 4)

Label for Omeprazole Delayed-Release Capsules, USP, 40 mg, oral capsule dosage form. The label includes storage and usage instructions, distributor information for Lannett Company, Inc., and specifies a 30-capsule count. It also features a barcode and a Lannett logo.*

* 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.