Losartan Potassium And Hydrochlorothiazide
Product Images NDC 68258-6040

View Photos of 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)
This is a product description of Losartan Potassium/HCTZ XX (100 mg/25 mg*) Tablets. The tablets are white to off-white and are film-coated, capsule-shaped, and have ZD19 written on them. They are distributed by Zydus Pharmaceuticals USA Inc. and the product ID is 6040-X. These tablets are dispensed orally, and patients should take ___ tablet(s) ___ time(s) a day as directed by their physician. The MFR. LOT number is not given. The product is packed in a tight/light-resistant container, and patients should not discontinue usage without a physician's advice. Dizziness or drowsiness may occur. The tablets contain 100 mg of Losartan Potassium USP and 25 mg of Hydrochlorothiazide USP. A warning is given that use during pregnancy can cause fetal harm, and it is marked RX only. The tablets should be kept out of children's reach and stored between 68°- 77° F. The packaged by address is Santa Ana, CA 92704.*
FDA Label Image

Structured Formula For Losartan (Losartan Hydro Figure 01)

FDA Label Image

Structured Formula For Losartan (Losartan Hydro Figure 02)

* 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.