Structural Formula (Benicar Hct 01)
Benicar Hct Tablet, Film Coated
Product Images NDC 0713-0865
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Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Benicar Hct (NDC 0713-0865). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Cosette Pharmaceuticals, 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.
Hctz Structure (Benicar Hct 02)
Principal Display Panel Ndc 0713-0863-30 Tablets Benicar Hct (olmesartan Medoxomil And Hydrochlorothiazide) 20 mg / 12.5 mg 30 Tablets Rx Only (Benicar Hct 03)
This is a medication description for a product called BenicarHCT, which contains olmesartan medoxomil and hydrochlorothiazide. The dosage and usage information can be found in the package insert and the product should be stored at room temperature. The product is marketed by Cosette Pharmaceuticals and comes from Germany. The NDC number is 0713-0863-30.*
Principal Display Panel Ndc 0713-0864-30 Tablets Benicar Hct (olmesartan Medoxomil And Hydrochlorothiazide) 40 mg / 12.5 mg 30 Tablets Rx Only (Benicar Hct 04)
This is a description of a pharmaceutical product named BenicarHCT. It is a tablet containing active ingredients such as olmesartan medoxomil and hydrochlorothiazide. The dosage and use instructions are mentioned on the package insert, and the tablet must be stored at a temperature of 20-25°C (68-77°F). It is marketed by Cosette Pharmaceuticals and produced in Germany. The NDC code of this product is 0713-0864-30.*
Principal Display Panel Ndc 0713-0865-30 Tablets Benicar Hct (olmesartan Medoxomil And Hydrochlorothiazide) 40 mg / 25 mg 30 Tablets Rx Only (Benicar Hct 05)
* 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.
