Lisinopril Tablet
Product Images NDC 42708-165

3 FDA label images from Qpharma, 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 Lisinopril (NDC 42708-165). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qpharma, 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.

Product Images & Figures Index

FDA Label Image

Lisinopril (6723a96d 02f8 40c2 95ec 89a7053a7117 01)

Lisinopril (6723a96d 02f8 40c2 95ec 89a7053a7117 01)
Chemical structure of Lisinopril dihydrate, depicting its molecular arrangement including functional groups and water molecules associated (2H2O). This image visually represents the active ingredient in the Lisinopril 20 mg oral tablet by QPharma, Inc.*
FDA Label Image

Image (94427465 A390 4ef9 866e 0669e7a6d3eb 806 1)

Image (94427465 A390 4ef9 866e 0669e7a6d3eb 806 1)
Lisinopril 20 mg oral tablets packaging label from QPharma, Inc. The label features the product name and strength prominently, with a stylized molecular diagram in black and white as a central graphic element. The design is clean, focusing on the product identification for prescription use.*
FDA Label Image

Label (42708 165 30 Label)

Label (42708 165 30 Label)
Label for Lisinopril Tablets USP, 20 mg, oral tablet dosage form, containing 30 tablets. The label includes directions for use with blanks to fill in dosage and frequency. The product is distributed by QPharma, Inc., Cedar Knolls, NJ, and is marked Rx Only. Storage instructions indicate keeping at controlled room temperature and out of reach of children.*

* 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.