Lisinopril And Hydrochlorothiazide
Product Images NDC 61919-308

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 Lisinopril And Hydrochlorothiazide (NDC 61919-308). 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

Image Description (Module1)

Image Description (Module1)
Chemical structure diagram of Lisinopril. The structure shows the arrangement of atoms in the Lisinopril molecule along with associated water molecules indicated as 2H2O.*
FDA Label Image

Image Description (Lisinhydro308)

Image Description (Lisinhydro308)
The packaging label for LISINOPRIL AND HYDROCHLOROTHIAZIDE 20/12.5mg tablets by DIRECT RX displays a count of 30 tablets. The label indicates it is the generic form of ZESTORIC with each tablet containing Lisinopril and Hydrochlorothiazide, USP 20/12.5 mg. The label includes lot and discard information, warnings about drug transfer and child safety, and advises against drinking alcohol or driving when using this medication. The label has a yellow highlight behind the main drug name and strength.*
FDA Label Image

Image Description (Module 2)

Image Description (Module 2)
Chemical structure of the active ingredient in LISINOPRIL AND HYDROCHLOROTHIAZIDE by DIRECT RX. The diagram shows a molecular structure with rings, chlorine, sulfur, nitrogen, and oxygen atoms arranged in a specific pattern indicative of the combined pharmaceutical compound.*

* 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.