Omeprazole Capsule, Delayed Release
Product Images NDC 67296-1939

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 67296-1939). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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)

Folding carton label for Omeprazole delayed-release capsules, USP 40 mg, Rx only. The label includes quantity information of 12 x 30 capsules, pharmacist dispensing guidance, and storage instructions. The label features a barcode and the Dr. Reddy's logo with their contact information. The carton design includes a purple semicircle accent on the right side.*

FDA Label Image

Dcontainer (Dcontainer)

Packaging label for Omeprazole delayed-release capsules USP, 40 mg strength, containing 30 capsules. The label includes usage and storage instructions, with the product labeled as Rx only. The label also features the Dr. Reddy's logo and a barcode.*

FDA Label Image

Carton1 (Carton1)

Box 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), with storage instructions, usage directions, and a note that the capsules should be swallowed whole without crushing. The label also includes a barcode and instructions for pharmacists to dispense the medication guide to patients.*

FDA Label Image

Carton2 (Carton2)

Packaging label for Omeprazole Delayed-Release Capsules USP, 20 mg, 7 capsules per box. The label includes dosage form as delayed-release capsules and notes that the product is by Dr. Reddy's Laboratories, manufactured in India. The label also provides usual adult dosage instructions and storage conditions, highlighting the product is prescription only.*

FDA Label Image

Carton3 (Carton3)

The packaging label for Omeprazole Delayed-Release Capsules USP, 40 mg, shows a carton for 100 capsules (10 x 10 unit-dose). The label specifies it is an oral prescription drug by Dr. Reddy's Laboratories Limited and includes storage instructions, dosage form, and a note that the unit-dose package is not child-resistant. The labeler is Redpharm Drug and the NDC is partially visible.*

FDA Label Image

Container1 (Container1)

Packaging label for Omeprazole Delayed-Release Capsules, USP 10 mg, containing 100 capsules. The label is Rx only and includes dispensing instructions for pharmacists. The product is labeled with NDC 55111-643-01 and manufactured by Dr. Reddy's Laboratories.*

FDA Label Image

Container2 (Container2)

Label for Omeprazole Delayed-Release Capsules USP 20 mg by Dr. Reddy's. The label indicates 100 capsules per container and includes usage instructions to dispense the medication guide to each patient. It also provides storage conditions and a QR code for the medication guide. The label features the NDC code and barcode.*

FDA Label Image

Container3 (Container3)

Packaging label for Omeprazole delayed-release capsules, USP 40 mg, containing 100 capsules. The label includes dosage form, strength, quantity, directions to dispense the Medication Guide, and storage instructions. It also features the Dr. Reddy's logo and barcode, along with a QR code linking to the medication guide.*

FDA Label Image

Structure (Structure)

Chemical structure of Omeprazole, showing the molecular arrangement of its atoms and bonds as two linked aromatic rings with specific functional groups, including methoxy and sulfoxide moieties.*

* 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.