Losartan Potassium And Hydrochlorothiazide Tablet, Film Coated
Product Images NDC 68788-8187

3 FDA label images from Preferred Pharmaceuticals Inc. · 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 Losartan Potassium And Hydrochlorothiazide (NDC 68788-8187). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Preferred 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.

FDA Label Image

Losartan Potassium And Hctz Tablets 50mg/12.5mg (46cf633d 70a5 4d3b B349 Ad74c23ddace 00)

Losartan Potassium And  Hctz Tablets 50mg/12.5mg (46cf633d 70a5 4d3b B349 Ad74c23ddace 00)
Label for Losartan Potassium & HCTZ Tablets 50 mg/12.5 mg, film-coated tablets, generic for Hyzaar. The label includes dosing directions in English and Spanish, manufacturer Solco Healthcare U.S., LLC, Cranbury, NJ, and storage warnings. It also features a barcode and a QR code, plus spaces for prescription details and lot numbers. Labeler is Preferred Pharmaceuticals Inc.*
FDA Label Image

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

73c71ed3-figure-01 (73c71ed3 Figure 01)
Chemical structure of losartan potassium, showing detailed molecular bonds and atomic arrangement typical of this active ingredient in pharmaceutical formulations.*
FDA Label Image

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

73c71ed3-figure-02 (73c71ed3 Figure 02)
Chemical structure of losartan potassium, showing its molecular components including a chlorinated aromatic ring, sulfonamide group, and other characteristic functional groups.*

* 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.