Omeprazole Capsule, Delayed Release
Product Images NDC 68462-396

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 68462-396). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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

Lbl10mg90s

Lbl10mg90s
Omeprazole 10 mg delayed-release capsules, USP, packaged by Glenmark Pharmaceuticals Inc. The label indicates 90 capsules per container for oral use as prescription medication. It includes dosage instructions, storage conditions, and a barcode, with labeler information showing Glenmark Pharmaceuticals, USA and India.*
FDA Label Image

Lbl20mg90s

Lbl20mg90s
The label for Omeprazole Delayed-Release Capsules, USP 20 mg by Glenmark Pharmaceuticals Inc., USA. It states the dosage form as capsules in a package of 90 count, intended for oral use. The label includes a barcode, storage instructions, and prescription-only status, emphasizing not to chew or crush the capsules.*
FDA Label Image

Lbl40mg100s

Lbl40mg100s
Label for Omeprazole Delayed-Release Capsules, USP 40 mg by Glenmark Pharmaceuticals Inc., USA. The label indicates Rx only and contains 100 capsules. Instructions note dispensing the Medication Guide separately to each patient. Storage and dosing information, barcode, and manufacturer details are also included.*
FDA Label Image
FDA Label Image

Image-01 (Image 01)

Image-01 (Image 01)
Chemical structure of Omeprazole, showing its molecular arrangement with characteristic functional groups including methoxy, sulfoxide, and benzimidazole rings.*

* 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.