Lisinopril And Hydrochlorothiazide
Product Images NDC 70934-718

3 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · 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 70934-718). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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

Figure 1 (Af83fd80 323e 45c6 9ec0 Df1845293bed 01)

Figure 1 (Af83fd80 323e 45c6 9ec0 Df1845293bed 01)
Chemical structure diagram of lisinopril dihydrate, showing its molecular composition and arrangement of atoms, represented with common organic chemistry notation.*
FDA Label Image

Figure 2 (Af83fd80 323e 45c6 9ec0 Df1845293bed 02)

Figure 2 (Af83fd80 323e 45c6 9ec0 Df1845293bed 02)
Chemical structure diagram of hydrochlorothiazide, an active ingredient in Lisinopril and Hydrochlorothiazide. The diagram shows the molecular arrangement including chlorine, sulfonamide, and other groups, represented by standard chemical notation symbols.*
FDA Label Image

Label (70934 718 90 Master Bottle Label Approval Rev A 05 20)

Label (70934 718 90 Master Bottle Label Approval   Rev A 05 20)
Label for Lisinopril and Hydrochlorothiazide Tablets USP 20mg/25mg by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The label states the NDC 70934-718-90 and package contains 90 tablets. Storage instructions include maintaining temperature at 20°-25°C and protection from light and humidity. It is marked Rx Only with standard warnings about keeping out of reach of children and storing in the original container.*

* 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.