Omeprazole Capsule, Delayed Release
Product Images NDC 68462-397

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 68462-397). 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

Structure (Image 01)

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

FDA Label Image

Logo1 (Logo1)

FDA Label Image

Logo2 (Logo2)

FDA Label Image

Label10mg90s (Label10mg90s)

Label for Omeprazole Delayed-Release Capsules, USP 10 mg, packaged by Glenmark Pharmaceuticals Inc., USA. The label indicates a quantity of 90 capsules and includes dispensing instructions, storage conditions, and contact information for the manufacturer. The label features barcodes and notes that this is a prescription-only medication.*

FDA Label Image

Label20mg90s (Label20mg90s)

Label for Omeprazole delayed-release capsules, USP 20 mg by Glenmark Pharmaceuticals Inc., USA. The label states 'Rx only' and indicates a package containing 90 capsules. It includes storage instructions, dosage caution, pharmacist dispensing guidance, and contact information with a barcode.*

FDA Label Image

Label40mg100s (Label40mg100s)

Omeprazole Delayed-Release Capsules, USP 40 mg label from Glenmark Pharmaceuticals Inc., USA. The label shows a white and yellow color scheme with black text. It states the product is for prescription use only and contains 100 capsules. Storage instructions and distributor contact information are also included.*

* 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.