Clonidine Hydrochloride Tablet, Extended Release
Product Images NDC 72162-1367

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonidine Hydrochloride (NDC 72162-1367). 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 molecular diagram with chloride (Cl) atoms and a hydrochloride (HCl) group in the structure.*

FDA Label Image

Clonidine-02.jpg (Clonidine 02)

A pharmacokinetic graph showing mean plasma concentrations (pg/mL) of Clonidine Hydrochloride over 48 hours. It compares extended-release tablets under fasted and fed conditions, and immediate-release tablets under fasted conditions, with time in hours on the x-axis and concentration on the y-axis.*

FDA Label Image

Clonidine-03.jpg (Clonidine 03)

A line graph showing the estimated proportion of patients with treatment failure over time in days from randomization. It compares Clonidine Hydrochloride Extended-Release Tablet (solid red line) and placebo (dashed black line) with censored data points marked by plus signs. The graph illustrates treatment failure rates up to approximately 220 days.*

FDA Label Image

Label (Lbl721621367)

Label for Clonidine Hydrochloride Extended-Release Tablets, 0.1 mg per tablet, oral dosage form. The label shows the product is relabeled by Bryant Ranch Prepack, Inc., Burbank, CA, and manufactured by Xiamen LP Pharmaceutical Co., Ltd. The label includes storage instructions and warnings about tablet use, with a package size of 60 tablets and NDC 72162-1367.*

* 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.