Lisinopril
Product Images NDC 10544-585

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lisinopril (NDC 10544-585). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Label (Label Lisinopril Tabs 2 5mg Bpi(10544 623 30) Qualitest(0603 4209 28) Rev1 Copy)

Lisinopril Tablets USP 2.5 mg label from Blenheim Pharmacal, Inc. The label specifies 30 tablets per package, Rx only, with storage instructions to keep at controlled room temperature (20°-25°C) and protect from moisture and freezing. It includes the NDC 10544-623-30, manufacturer code 0603-4209-28, and placeholders for lot and expiration dates. The right side shows peelable sections with repeating product information for pharmacy use.*

FDA Label Image

Label (Label Lisinopril Tabs 5mg Bpi(10544 585 30) Qualitest(0603 4210 32) Rev1)

Lisinopril Tablets, USP 5mg label for a 30-tablet bottle by Blenheim Pharmacal, Inc. The label includes NDC 10544-585-30 and manufacturing code 0603-4210-32. Storage instructions advise protecting from moisture and freezing, keeping at controlled room temperature 20-25°C (68-77°F), and storing in a light-resistant container out of reach of children. The package is marked Rx Only with dosage directions to see the package insert.*

FDA Label Image

Structure (Lisin 1)

Chemical structure of the active ingredient Lisinopril, depicting its molecular arrangement with functional groups including carboxyl, amine, and a cyclic ring, along with two water molecules (dihydrate).*

* 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.