Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 70518-3420

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Losartan Potassium And Hydrochlorothiazide (NDC 70518-3420). 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)

Chemical structure of losartan potassium, showing its molecular composition including a potassium ion, chlorine, and various organic groups. The structure represents the active ingredient of Losartan Potassium and Hydrochlorothiazide tablets.*

FDA Label Image

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

Chemical structure diagram of the active ingredient losartan potassium, showing its molecular arrangement with specified functional groups and atoms.*

FDA Label Image

Mm2 (Losartan Potassium Hctz 100mg 25mg 70518 3420 01)

Label for Losartan Potassium and Hydrochlorothiazide 100 mg / 25 mg oral film-coated tablet. The label includes directions to see the package insert, storage instructions, and notes that it is repackaged by RemedyRepack Inc. The label shows the quantity of 1 tablet and displays the NDC 70518-3420-01 along with manufacturing information from Solco in Cranbury, NJ.*

FDA Label Image

Remedy_label (Remedy Label)

Label for Losartan Potassium and Hydrochlorothiazide 100 mg/25 mg film-coated tablets. The label indicates a quantity of 30 tablets, Rx only, with NDC 70518-3420-00. Manufactured by Solco, Cranbury, NJ, and repackaged by RemedyRepack Inc. Directions refer to package insert. Storage conditions and safety warnings are included.*

* 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.