Omeprazole Capsule, Delayed Release
Product Images NDC 55111-645

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 55111-645). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories Limited, 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

Dcarton (Dcarton)

Packaging label for Omeprazole delayed-release capsules 40 mg by Dr. Reddy's Laboratories Limited. The label indicates a package containing 12 bottles with 30 capsules each. It includes prescription-only status and storage instructions, as well as a barcode and a purple design element on a white background.*

FDA Label Image

Dcontainer (Dcontainer)

Label for Omeprazole Delayed-release Capsules, USP 40 mg by Dr. Reddy's Laboratories Limited. The label shows a bottle containing 30 capsules and includes usage instructions, storage information, a QR code for medication guide, and the NDC number 55111-645-34. The label is primarily white with blue and purple text.*

FDA Label Image

Carton1 (Carton1)

Packaging label for Omeprazole delayed-release capsules, 10 mg, manufactured by Dr. Reddy's Laboratories Limited. The label indicates 100 capsules (10 x 10 unit-dose) and includes storage instructions and a caution that the unit-dose package is not child-resistant. The label also states the capsules are for oral use and require a pharmacist to dispense a medication guide to each patient.*

FDA Label Image

Carton2 (Carton2)

Packaging label for Omeprazole delayed-release capsules USP, 20 mg by Dr. Reddy's Laboratories Limited. The label indicates the product contains 7 capsules (7 unit-dose) and includes instructions to dispense the medication guide to each patient. Storage instructions and usual adult dosage guidance are provided, with a note that the unit-dose package is not child-resistant.*

FDA Label Image

Carton3 (Carton3)

Packaging label for Omeprazole delayed-release capsules USP 40 mg by Dr. Reddy's Laboratories Limited. The label indicates prescription use, with a package quantity of 100 capsules (10 bottles of 10 capsules each). Storage instructions specify 20° to 25°C (68° to 77°F). Additional information includes dosage instruction emphasis and child-resistant packaging note.*

FDA Label Image

Container1 (Container1)

Label for Omeprazole Delayed-Release Capsules, USP 10 mg by Dr. Reddy's Laboratories Limited. The label indicates the product is prescription only, packaged as 100 capsules, and includes usage instructions along with a barcode and a QR code for medication guide access.*

FDA Label Image

Container2 (Container2)

Label for Omeprazole Delayed-Release Capsules, USP 20 mg by Dr. Reddy's Laboratories Limited. The label indicates a 100 capsule count. It includes pharmacist dispensing instructions, storage conditions, and a QR code for medication guide access. The label design features a large purple semi-circle and bar code.*

FDA Label Image

Container3 (Container3)

Label for Omeprazole delayed-release capsules USP 40 mg, oral dosage form, in a package of 100 capsules. Label includes directions for pharmacists to dispense the medication guide, storage instructions, and manufacturer details for Dr. Reddy's Laboratories Limited. The label also displays the NDC 55111-645-01 and a QR code for accessing the medication guide online.*

FDA Label Image

Structure (Structure)

Chemical structure of Omeprazole, a human prescription drug. The diagram shows the molecular arrangement including functional groups such as methoxy and sulfoxide moieties corresponding to the Omeprazole molecule.*

* 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.