Losartan Potassium And Hydrochlorothiazide
Product Images NDC 61919-797

3 FDA label images from Direct Rx · 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 61919-797). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

732 90

732 90
Packaging label for LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE 100 mg/12.5 mg tablets, containing 90 tablets. The label indicates the product is generic for Hyzaar, is packaged and distributed by Direct Rx in Alpharetta, GA, with NDC 61919-732-90. Additional warnings about potential side effects and a discard date are present.*
FDA Label Image

785 90

785 90
LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE 100/12.5 mg 90 Tablets packaged and distributed by DIRECT RX. The label indicates it is a generic for HYZAAR, with each tablet containing 100 mg losartan potassium USP and 12.5 mg hydrochlorothiazide USP. The label includes lot, expiration date, and manufacturer information along with warnings and directions for use.*
FDA Label Image

797 30

797 30
Label for LOSARTAN POT/HCTZ 100/12.5 mg tablets, 30 count, distributed by Direct Rx. The label indicates the product is a generic for Hyzaar, containing 100 mg Losartan potassium and 12.5 mg hydrochlorothiazide per film-coated tablet, with lot number and expiration date details 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.