Clonidine Hydrochloride
Product Images NDC 63629-1208

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonidine Hydrochloride (NDC 63629-1208). 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.

FDA Label Image

Structural Formula (Clonidine 01)

Chemical structure of Clonidine Hydrochloride showing a dichlorobenzene ring connected to an imidazoline ring, with the hydrochloride salt indicated.*

FDA Label Image

Clonidine-02.jpg (Clonidine 02)

A pharmacokinetic line graph showing mean plasma concentration (pg/mL) versus time (hours) for Clonidine Hydrochloride. It compares extended-release tablets taken fasted and fed, and immediate-release tablets taken fasted, illustrating their concentration profiles over 48 hours.*

FDA Label Image

Clonidine-03.jpg (Clonidine 03)

A Kaplan-Meier survival curve comparing Clonidine Hydrochloride Extended-Release Tablet and placebo for estimated proportion of patients with treatment failure over days from randomization to treatment failure. The graph includes censored data markers and shows treatment failure proportions on the y-axis and days on the x-axis.*

FDA Label Image

Label (Lbl636291208)

Label for Clonidine Hydrochloride ER Tablets, USP 0.1 mg by Bryant Ranch Prepack. The label includes NDC 63629-1208-1, a barcode, and storage instructions. It indicates 60 tablets per bottle and states Rx only. The label specifies that each tablet contains 0.1 mg Clonidine Hydrochloride and includes child-resistant container and temperature storage guidelines.*

* 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.