Lisinopril And Hydrochlorothiazide
Product Images NDC 53808-0451

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Lisinopril And Hydrochlorothiazide (NDC 53808-0451). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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 Image For 10mg (Lisinopril 10mg(lupin))

Label for Lisinopril 10 mg tablets, quantity 30, prescription only. Manufactured and packaged by DOH Central Pharmacy in Tallahassee, FL. The label includes lot number, expiration date, and a barcode with UPC# 368180514039.*

FDA Label Image

Label Image For 5mg (Lisinopril 5mg(lupin))

Packaging label for Lisinopril 5 mg tablets, quantity 30, labeled as RX only. The label lists the lot number 186477A and expiration date 09/30/2010. The product is packaged by DOH Central Pharmacy, Tallahassee, FL 32304, with a barcode and UPC number 368180513032 shown.*

FDA Label Image

Figure 1 (Lisinopril Figure 01)

Chemical structure diagram representing the active ingredients or components related to the product Lisinopril and hydrochlorothiazide by State of Florida DOH Central Pharmacy. The structure includes molecular bonds and specific chemical groups depicted by labeled atoms and bonds.*

FDA Label Image

Figure 2 (Lisinopril Figure 02)

Chemical structure diagram depicting a sulfonamide compound with a chlorinated aromatic ring and a six-membered heterocyclic ring containing nitrogen and a sulfonyl group. The image shows atomic connectivity and double-bonded oxygen atoms typically seen in drug molecular structures.*

* 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.