Omeprazole Capsule, Delayed Release
Product Images NDC 16714-630

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 16714-630). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

Container1 (Container1)

This is a product label for Omeprazole Delayed-Release Capsules, USP manufactured by NorthStar Rx LLC. Each capsule contains 40 mg of Omeprazole USP and is intended for adults. The medication is to be swallowed whole and is not to be opened, chewed, or crushed. The package insert contains dosage and prescribing information. The container should be stored at 20°C to 25°C and protected from light and moisture. A medication guide is available through the manufacturer's website or by phone.*

FDA Label Image

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Omeprazole Delayed-Release Capsules, U are available in 100 capsules and contain 20 mg of Omeprazole USP. The recommended usage is to swallow the capsule whole without opening, chewing or crushing it. A pharmacist should dispense the medication along with proper dosage information, and medication guides are available on the website of NorthStar Rx LLC, or by phone. The medicine should be kept at controlled room temperature and protected from moisture and light. The manufacturer is Dr. Reddy's Laboratories Limited based in India.*

FDA Label Image

Structure (Structure)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.