Guanfacine Hydrochloride Tablet
Product Images NDC 65162-711

View Photos of 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 Guanfacine Hydrochloride (NDC 65162-711). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, 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

042bf3b6-figure-01 (Guanfacine Tablets Usp 1)

042bf3b6-figure-01 (Guanfacine Tablets Usp 1)
Chemical structure of Guanfacine Hydrochloride showing its molecular composition with two chlorine atoms, amide, and guanidine functional groups, plus the associated hydrochloride (HCl).*
FDA Label Image

1 mg Label (Guanfacine Tablets Usp 2)

1 mg Label (Guanfacine Tablets Usp 2)
Label for Guanfacine Tablets, USP 1 mg by Amneal Pharmaceuticals LLC. The label states the dosage form as tablets with 30 count, prescription only. It includes storage instructions, dispensing directions, and distributor information from Amneal Pharmaceuticals in Bridgewater, NJ. The tablet imprint is displayed as '711'.*
FDA Label Image

2 mg Label (Guanfacine Tablets Usp 3)

2 mg Label (Guanfacine Tablets Usp 3)
Label for Guanfacine Tablets USP, 2 mg strength, oral tablets. The label indicates the product contains 30 tablets and is distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ. Storage instructions specify 20° to 25°C (68° to 77°F) and recommend a tight, light-resistant container with child-resistant closure. The NDC is 65162-713-03.*

* 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.