Omeprazole Capsule, Delayed Release
Product Images NDC 55111-157

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 55111-157). 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, USP 20 mg by Dr. Reddy's Laboratories Limited. The carton indicates the product contains 12 bottles of 30 capsules each with directions and storage instructions. Label includes a barcode and states 'Rx Only.'*

FDA Label Image

Dcontainer (Dcontainer)

Label for Omeprazole Delayed-release Capsules, USP 20 mg, bulk packaging containing 30 capsules. The label includes usage instructions for medical professionals, barcode, QR code for medication guide, and states the labeler as Dr. Reddy's Laboratories Limited, batch number, and storage conditions.*

FDA Label Image

Carton1 (Carton1)

Packaging label for Omeprazole Delayed-release Capsules USP 10 mg by Dr. Reddy's Laboratories Limited. The package contains 100 capsules (10 blister packs of 10). The label includes dosing instructions, storage conditions, and a note that this unit dose package is not child-resistant. The manufacturer is located in Bachupally, India.*

FDA Label Image

Carton2 (Carton2)

Packaging label for Omeprazole delayed-release capsules USP, 20 mg, as bulk ingredient by Dr. Reddy's Laboratories Limited. The label specifies a unit dose package containing 100 capsules (10 x 10). It includes dosage instructions, storage conditions, and states Rx only. The label features the manufacturer information and bar code.*

FDA Label Image

Carton3 (Carton3)

Packaging label for Omeprazole delayed-release capsules USP, 40 mg. The label indicates unit dose packaging with 100 capsules (10 x 10). It includes instructions to dispense the medication guide to each patient, storage instructions, and manufacturer details for Dr. Reddy's Laboratories Limited, India. The label also notes the capsules should be swallowed whole and not opened, chewed, or crushed.*

FDA Label Image

Container1 (Container1)

Label for Omeprazole Delayed-release Capsules, USP 10 mg, a bulk ingredient dosage form. The label displays the strength (10 mg), quantity (30 capsules), and directs pharmacists to dispense the medication guide. It shows the NDC 55111-157-30 and is labeled by Dr. Reddy's Laboratories Limited. Additional storage and usage instructions are partially visible.*

FDA Label Image

Container2 (Container2)

Label for Omeprazole delayed-release capsules, USP 20 mg by Dr. Reddy's Laboratories Limited. The label indicates Rx only and contains 30 capsules. It includes a National Drug Code (NDC) 55111-158-30, barcode, medication guide reference, and storage instructions. The layout uses blue and red text on a white background.*

FDA Label Image

Container3 (Container3)

Packaging label for Omeprazole Delayed-release Capsules USP 40 mg by Dr. Reddy's Laboratories Limited. The label indicates a package containing 30 capsules, marked Rx Only. It includes dosage form, strength, instructions for pharmacists to dispense the Medication Guide, storage conditions, and a barcode with an NDC number 55111-159-30.*

FDA Label Image

Structure (Structure)

Chemical structure of Omeprazole, a bulk ingredient in delayed-release capsule form. The diagram shows molecular components including aromatic rings, sulfur, nitrogen, oxygen, and methyl groups characteristic of Omeprazole's chemical makeup.*

* 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.