Omeprazole Capsule, Delayed Release
Product Images NDC 59651-003

7 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 59651-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (10 mg (30 Capsule Bottle))

Package Label-principal Display Panel (10 mg (30 Capsule Bottle))
Label for Omeprazole Delayed-Release Capsules, USP 10 mg by Aurobindo Pharma Limited. The label states this product is Rx only and contains 30 capsules. It includes storage instructions, distributor information, and a barcode on the right side. The label also notes the capsules are enteric-coated granules and made in India.*
FDA Label Image

Package Label-principal Display Panel (10 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (10 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Omeprazole Delayed-Release Capsules, USP, 10 mg strength, distributed by Aurobindo Pharma Limited. The label shows unit-dose capsules in a 100-count package (10 x 10). The design includes the NDC number 59651-001-78 and directions for pharmacists to dispense the Medication Guide separately.*
FDA Label Image

P1420940 Omeprazole Dr Capsules Usp 20 mg (30's) Label (Omeprazole Fig3)

P1420940 Omeprazole Dr Capsules Usp 20 mg (30's) Label (Omeprazole Fig3)
Label for Omeprazole Delayed-Release Capsules USP 20 mg, with 30 capsules per package. The label states the product is Rx only and contains omeprazole as enteric-coated granules. It includes storage instructions, distributor information for Aurobindo Pharma USA, and a barcode. The label is marked for the labeler Aurobindo Pharma Limited and indicates it is made in India.*
FDA Label Image

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Omeprazole Delayed-Release Capsules USP 20 mg by Aurobindo Pharma Limited. The label indicates 100 unit-dose capsules (10 x 10) with a green 20 mg strength marker. It includes usage instructions for pharmacists, storage information, and barcodes. The product type is delayed-release capsules.*
FDA Label Image

P1420945 Omeprazole Dr Capsules Usp 40 mg (30's) Label (Omeprazole Fig5)

P1420945 Omeprazole Dr Capsules Usp 40 mg (30's) Label (Omeprazole Fig5)
Label for Omeprazole Delayed-Release Capsules, USP 40 mg by Aurobindo Pharma Limited. The label indicates the product is Rx only, contains 30 capsules, and each delayed-release capsule contains 40 mg omeprazole as enteric-coated granules. It includes storage instructions at controlled room temperature and advisory notes for pharmacists and consumers. Distributed by Aurobindo Pharma USA, Inc.*
FDA Label Image

P1029610 Omeprazole Dr Capsules Usp 40mg (10 X 10's) Carton (Omeprazole Fig6)

P1029610 Omeprazole Dr Capsules Usp 40mg (10 X 10's) Carton (Omeprazole Fig6)
Packaging label for Omeprazole Delayed-Release Capsules USP, 40 mg, distributed by Aurobindo Pharma Limited. The label indicates the product is Rx only and includes 100 unit-dose capsules (10 x 10). It features directions for pharmacists to dispense the medication guide separately and specifies the capsule contains enteric-coated granules of Omeprazole USP 40 mg.*
FDA Label Image

Chemical Structure (Omeprazole Str)

Chemical Structure (Omeprazole Str)
Chemical structure of Omeprazole, showing two connected heterocyclic rings with various substituents including methoxy, methyl, sulfinyl, and nitrogen-containing 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.