Lisinopril And Hydrochlorothiazide
Product Images NDC 63629-8083

3 FDA label images from Bryant Ranch Prepack · 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 63629-8083). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structural Formula Of Lisinopril (Image 1)

Structural Formula Of Lisinopril (Image 1)
Chemical structure diagram showing the molecular formula of Lisinopril and Hydrochlorothiazide, including annotated atoms and bonds with water of hydration (2H2O) indicated.*
FDA Label Image

Structural Formula Of Hydrochlorothiazide (Image 2)

Structural Formula Of Hydrochlorothiazide (Image 2)
Chemical structure diagram showing a compound with a benzene ring substituted with chlorine and sulfonamide groups, connected to a heterocyclic ring containing nitrogen and sulfone groups. This represents a molecular structure likely relevant to the active ingredients in the product Lisinopril and Hydrochlorothiazide.*
FDA Label Image

Label Image (Lbl636298083)

Label Image (Lbl636298083)
Packaging label for Lisinopril and Hydrochlorothiazide 20-12.5 mg tablets from Bryant Ranch Prepack. The label indicates the product is compared to Zestoretic 20-12.5 mg tablets by Watson Pharma Private Limited. It includes storage instructions to keep at 20°-25°C (68°-77°F) and a warning to keep out of reach of children. The package contains 30 tablets with NDC 63629-8083.*

* 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.