Olmesartan Medoxomil Tablet, Film Coated
Product Images NDC 72303-0848

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Olmesartan Medoxomil (NDC 72303-0848). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hec Pharm Usa Inc., 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

20mg-30tabs (20mg 30tabs)

20mg-30tabs (20mg 30tabs)
Packaging label for Olmesartan Medoxomil Tablets, USP 20 mg film-coated tablets. The label indicates a package size of 30 tablets, labeled by HEC Pharm USA Inc., with manufacturing by Sunshine Lake Pharma Co., Ltd. The label includes storage instructions and a barcode.*
FDA Label Image

20mg-90tabs (20mg 90tabs)

20mg-90tabs (20mg 90tabs)
Label for Olmesartan Medoxomil Tablets, USP 20 mg, film-coated oral tablets. The label states the active ingredient is olmesartan medoxomil 20 mg per tablet. It indicates the manufacturer as Sunshine Lake Pharma Co., Ltd. in China and distributor as HEC Pharm USA Inc., Plainsboro, NJ. The package contains 90 tablets with the instruction for Rx only. Storage information and a barcode are also displayed.*
FDA Label Image

40mg-30tabs (40mg 30tabs)

40mg-30tabs (40mg 30tabs)
Label for Olmesartan Medoxomil Tablets, USP 40 mg film-coated tablets, containing 30 tablets per package. The label includes storage instructions, distributor HEC Pharm USA Inc., and manufacturer Sunshine Lake Pharma Co., Ltd. It features the NDC 72303-0850-1 and a barcode.*
FDA Label Image

40mg-90tabs (40mg 90tabs)

40mg-90tabs (40mg 90tabs)
Label for Olmesartan Medoxomil Tablets, USP 40 mg, oral film-coated tablets. The label indicates the product contains 90 tablets, is Rx only, and is distributed by HEC Pharm USA Inc. It includes storage instructions and manufacturer details (Sunshine Lake Pharma Co., Ltd., China). A barcode and NDC number 72303-0850-2 are visible.*
FDA Label Image

5mg-30tabs (5mg 30tabs)

5mg-30tabs (5mg 30tabs)
Label for Olmesartan Medoxomil Tablets, USP 5 mg oral film-coated tablets. The label indicates the product contains 30 tablets, is distributed by HEC Pharm USA Inc., and manufactured by Sunshine Lake Pharma Co., Ltd. Storage instructions and NDC 72303-0848-1 are also shown.*
FDA Label Image

5mg-90tabs (5mg 90tabs)

5mg-90tabs (5mg 90tabs)
Label for Olmesartan Medoxomil 5 mg film-coated tablets, USP, oral route, containing 90 tablets. The label includes dosage strength, uses, storage instructions, and manufacturer details. Distributed by HEC Pharm USA Inc., manufactured by Sunshine Lake Pharma Co., Ltd., China. Features NDC 72303-0848-2 and a barcode.*
FDA Label Image

Logo0001-01 (Logo0001 01)

FDA Label Image

Logo0001-02 (Logo0001 02)

FDA Label Image

Chemical Structure (Olmesartan Medoxomil Figure 1)

Chemical Structure (Olmesartan Medoxomil Figure 1)
Chemical structure of Olmesartan medoxomil, the active ingredient in OLMESARTAN MEDOXOMIL tablets. The diagram shows the molecular arrangement including rings, carbon chains, and functional groups characteristic of this compound.*
FDA Label Image

Figure (Olmesartan Medoxomil Figure 2)

Figure (Olmesartan Medoxomil Figure 2)
A line graph titled 'Olmesartan Medoxomil Dose Response Placebo-Adjusted Reduction In Blood Pressure (mmHg)' showing the relationship between Olmesartan Medoxomil dose (mg) on the x-axis and reduction in blood pressure (mmHg) on the y-axis. It includes two curves representing systolic and diastolic blood pressure reductions, with systolic showing greater reduction at higher doses.*

* 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.