Guanfacine Hydrochloride Tablet
Product Images NDC 72603-269

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 72603-269). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

1 mg Label (Guanfacine Tablets Usp 1mg 100s)

1 mg Label (Guanfacine Tablets Usp 1mg 100s)
Label for Guanfacine Tablets USP 1 mg oral tablets, containing 100 tablets per package. The label displays the NDC number 72603-268-01 and indicates the product is manufactured for Northstar RX LLC. Storage instructions specify controlled room temperature, and the packaging includes child-resistant closure.*
FDA Label Image

2 mg Label (Guanfacine Tablets Usp 2mg 100s)

2 mg Label (Guanfacine Tablets Usp 2mg 100s)
Label for Guanfacine Tablets, USP 2 mg oral tablets by Northstar Rx LLC. The package contains 100 tablets. The label states the active ingredient is guanfacine hydrochloride equivalent to 2 mg guanfacine, with storage instructions and manufacturer details including Chemo India Formulations Pvt. Ltd. in Hyderabad, India.*
FDA Label Image

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

042bf3b6-figure-01 (Guanfacine Tablets Usp Structure)
Chemical structure diagram of Guanfacine Hydrochloride, showing its molecular components including a dichlorophenyl group, a guanidine moiety, and associated hydrochloride component.*

* 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.