Omeprazole Capsule, Delayed Release
Product Images NDC 70518-3278

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 70518-3278). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Omeprazole 20mg 70518 3278 01

Omeprazole 20mg 70518 3278 01
Omeprazole 20 mg delayed-release capsules, quantity 30, repackaged by RemedyRepack Inc. The label shows the NDC number 70518-3278-01, manufacturing by Xiromed, LLC, Florham Park, NJ, and storage instructions at 20-25°C with permitted excursions. Contains QR codes and directions to see package insert for use details.*
FDA Label Image

Omeprazole 20mg 70518 3278 02

Omeprazole 20mg 70518 3278 02
Label for Omeprazole 20 mg delayed-release capsules, containing 90 capsules. The packaging identifies RemedyRepack Inc. as the repackager and includes storage instructions, a QR code, and directions to see the package insert for use information. The label states this is a prescription drug.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Omeprazole 20 mg delayed-release capsules label showing packaging for a quantity of 30 capsules. The label includes the NDC 70518-3278-00, repackaged by RemedyRepack Inc., and manufactured by Xiromed, LLC in Florham Park, NJ. Directions for use refer to the package insert and storage instructions are provided.*

* 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.