Lisinopril And Hydrochlorothiazide
Product Images NDC 70934-128

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 70934-128). 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.

Product Images & Figures Index

FDA Label Image

70934 128 30 Master Bottle Label Approval Rev B 10 19

70934 128 30 Master Bottle Label Approval Rev B 10 19
Label for Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg, 30 tablets, from Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The label includes dosage strength, quantity, Rx only status, storage instructions, and NDC 70934-128-30. Packaging information and manufacturer details are visible on the peel-off sheet along the right side.*
FDA Label Image

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

Figure 1 (Af83fd80 323e 45c6 9ec0 Df1845293bed 01)
Chemical structure diagram showing the molecular formula of lisinopril dihydrate, the active ingredient in Lisinopril and Hydrochlorothiazide by Denton Pharma, Inc. DBA Northwind Pharmaceuticals.*
FDA Label Image

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

Figure 2 (Af83fd80 323e 45c6 9ec0 Df1845293bed 02)
Chemical structure diagram of Hydrochlorothiazide, the active ingredient in Lisinopril and Hydrochlorothiazide by Denton Pharma, Inc. DBA Northwind Pharmaceuticals.*

* 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.