Omeprazole Delayed-release
Product Images NDC 63304-445

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Omeprazole Delayed-release (NDC 63304-445). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ranbaxy Laboratories 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

Container Label 1000s (Contain 1000s)

Label for Omeprazole Delayed-Release 40 mg capsules by Ranbaxy Laboratories Inc. The label indicates the product contains 1000 capsules, with storage instructions and a barcode present. Manufactured for Ranbaxy Pharmaceuticals Inc., Jacksonville, FL, and Merck & Co., Inc., Whitehouse Station, NJ.*

FDA Label Image

Container Label 100s (Contain 100s)

Omeprazole Delayed-Release Capsules 40 mg bottle label from Ranbaxy Laboratories Inc. The label includes storage instructions, a barcode, and notes that the package contains 100 capsules. It states the product is Rx only and provides manufacturer and distributor information.*

FDA Label Image

Container Label 30s (Contain 30s)

Label for Omeprazole Delayed-Release Capsules 40 mg by Ranbaxy Laboratories Inc. The label includes the 30-capsule count, the product NDC (63304-445-30), and storage instructions. It advises keeping the container tightly closed and storing between 15°C and 30°C (59°F and 86°F). Usage instructions note to swallow capsules whole without opening, chewing, or crushing. Manufacturer details for Ranbaxy Pharmaceuticals Inc. and Merck & Co., Inc. are also present.*

FDA Label Image

Chemical Structure (Structure)

Chemical structure diagram of the active ingredient Omeprazole showing its molecular framework with labeled functional groups.*

* 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.