Omeprazole Tablet, Delayed Release
Product Images NDC 59726-298

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 59726-298). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by P & L Development, 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

Omeprazole Delayed-release Tablet 20 mg (equivalent To 20.6 mg Omeprazole Magnesium (Omeprazole Magnesium Delayed Release Tablet Mia 1)

Omeprazole Delayed-release Tablet 20 mg (equivalent To 20.6 mg Omeprazole Magnesium (Omeprazole Magnesium Delayed Release Tablet Mia 1)
Drug Facts panel for Omeprazole delayed-release tablets, 20 mg. The text covers active ingredient, purpose, usage instructions, warnings including allergy alert and conditions when not to use, directions for adults, and additional information such as storage and inactive ingredients. The label mentions a 14-day course of treatment with 14 tablets total.*

* 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.