Olmesartan Medoxomil Tablet, Film Coated
Product Images NDC 72189-138

3 FDA label images from Direct Rx · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Olmesartan Medoxomil (NDC 72189-138). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

138 (72189 0138 30)

138 (72189 0138 30)
Olmesartan Medoxomil 40 mg film-coated tablets, packaged as a bottle containing 30 tablets. The label states it is generic for Benicar and indicates the active ingredient Olmesartan Medoxomil USP 40 mg per tablet. The product is packaged and distributed by Direct Rx.*
FDA Label Image

30 (72189 137 30)

30 (72189 137 30)
Olmesartan Medoxomil 20 mg film-coated tablets label with a package containing 30 tablets. The label indicates it is a generic for Benicar, distributed by direct rx, with lot number 11SE2002 and expiration date 6/30/21. The label shows multiple smaller labels with identical information for the same product and batch.*
FDA Label Image

137 (72189 137 90)

137 (72189 137 90)
Label for Olmesartan Medoxomil 20 mg film-coated tablets. The label states it contains 90 tablets and is generic for Benicar. The label includes the lot number 11SE2015, expiration date 12/31/21, and manufacturer/distributor listed as DIRECT Rx in Dawsonville, GA. National Drug Code (NDC) number 72189-137-90 is shown. The product is a prescription drug intended for oral use.*

* 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.