Omeprazole Capsule, Delayed Release
Product Images NDC 85509-1396

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Omeprazole (NDC 85509-1396). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Rx Llc, 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

Omeprazole Dr 20 mg Capsules (Omeprazole 1396 20mg)

Omeprazole Dr 20 mg Capsules (Omeprazole 1396 20mg)
This text provides information about Omeprazole delayed-release capsules containing 20 mg of the active ingredient. It includes instructions on dosage, storage conditions, and dispensing guidelines for pharmacists. The manufacturer is identified as Glenmark Pharmaceuticals Limited, and the repackager is PHOENIX RX LLC. The text also includes the National Drug Code (NDC) number, lot number (LOTX85), expiration date (July 10, 2026), and a GTIN code.*
FDA Label Image

Structure (Image 01)

FDA Label Image
FDA Label Image

Logo1 (Logo1)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.