Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 70518-3398

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 70518-3398). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

73c71ed3-figure-01 (73c71ed3 Figure 01)

73c71ed3-figure-01 (73c71ed3 Figure 01)
Chemical structure of losartan potassium, an active ingredient in the drug Losartan Potassium and Hydrochlorothiazide.*
FDA Label Image

73c71ed3-figure-02 (73c71ed3 Figure 02)

73c71ed3-figure-02 (73c71ed3 Figure 02)
Chemical structure of losartan potassium, the active ingredient in the drug Losartan Potassium and Hydrochlorothiazide. The diagram depicts the molecule's atomic and bonding arrangement, including rings and functional groups.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Losartan Potassium/HCTZ 100 mg/12.5 mg film-coated tablets in a 90-count package. The label shows the product name with strength, oral tablet form, and indicates it is prescription only. It is repackaged by RemedyRepack Inc., Indiana, PA, with storage information and references a package insert for directions.*

* 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.