Guanfacine Hydrochloride Tablet
Product Images NDC 60687-710

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Guanfacine Hydrochloride (NDC 60687-710). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp71021

Ahp71021
Guanfacine Hydrochloride 1 mg round white tablet imprinted with a 'U' on one side and '45' on the other. This oral tablet is manufactured by American Health Packaging.*
FDA Label Image

1 mg Guanfacine Tablet Blister (Blister)

1 mg Guanfacine Tablet Blister (Blister)
Multiple rectangular labels for Guanfacine Hydrochloride Tablet, USP 1 mg from American Health Packaging. Each label includes product name, strength (1 mg), dosage form (tablet), National Drug Code (60687-710-11-2), lot number placeholder, and expiry date placeholder. Labeler address in Columbus, Ohio is also shown.*
FDA Label Image

1 mg Guanfacine Tablets Carton (Carton)

1 mg Guanfacine Tablets Carton (Carton)
Label for Guanfacine Hydrochloride 1 mg oral tablets by American Health Packaging. The package contains 30 tablets (3 x 10) marked as prescription only. The label includes dosage form as tablets, strength as 1 mg, and storage instructions. It also lists the NDC 60687-710-21 and distributor information.*
FDA Label Image

Structural Formula (Structure)

Structural Formula (Structure)
Chemical structure of Guanfacine Hydrochloride, depicting a bicyclic ring with two chlorine atoms, connected to an amide and guanidine functional groups, alongside a 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.