Losartan Potassium And Hydrochlorothiazide
Product Images NDC 68258-6040

3 FDA label images from Dispensing Solutions, 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 68258-6040). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dispensing Solutions, 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

Ndc 68258-6040-xx (Ndc 68258 6040 Xx Zydus)

Ndc 68258-6040-xx (Ndc 68258 6040 Xx        Zydus)
Label for Losartan Potassium and Hydrochlorothiazide tablets, 100 mg/25 mg strength, distributed by Zydus Pharmaceuticals USA Inc. The label shows NDC 68258-6040 and highlights that each tablet contains 100 mg Losartan Potassium USP and 25 mg Hydrochlorothiazide USP. It includes warnings about pregnancy, storage conditions, and dosing instructions. The labeler is Dispensing Solutions, Inc., Santa Ana, CA.*
FDA Label Image

Structured Formula For Losartan (Losartan Hydro Figure 01)

Structured Formula For Losartan (Losartan Hydro Figure 01)
Chemical structure of losartan potassium, one of the active ingredients in LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE by Dispensing Solutions, Inc. The diagram depicts the molecular arrangement including the potassium ion.*
FDA Label Image

Structured Formula For Losartan (Losartan Hydro Figure 02)

Structured Formula For Losartan (Losartan Hydro Figure 02)
Chemical structure of the active ingredient in LOSARTAN POTASSIUM AND HYDROCHLORTHIAZIDE, showing a chlorinated benzene ring fused to a heterocyclic ring with sulfonamide and other 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.