Clonidine Hydrochloride Tablet, Extended Release
Product Images NDC 70069-044

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 Clonidine Hydrochloride (NDC 70069-044). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

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A line graph depicting mean concentration (pg/mL) over time (hours) for three conditions: Clonidine Hydrochloride under fasted and fed states, and Catapres under the fasted state. The graph shows concentration changes from 0 to 48 hours post-administration for each condition.*
FDA Label Image

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A Kaplan-Meier curve comparing the estimated proportion of patients with treatment failure over days from randomization. The graph plots two lines: a solid red line for Clonidine Hydrochloride and a black dashed line for placebo. The x-axis represents days from randomization to treatment failure (0 to 220 days), and the y-axis shows the estimated proportion of patients experiencing treatment failure (0.0 to 1.0). Censored data points are marked with plus signs on both curves.*
FDA Label Image

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Label for Clonidine Hydrochloride Extended-Release Tablets 0.1 mg, 60 count, from Somerset Therapeutics, LLC. The label states this is a prescription drug with NDC 70069-044-01, contains extended-release clonidine hydrochloride tablets, and is made in Portugal. Storage and handling instructions are included.*
FDA Label Image

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Chemical structure of Clonidine Hydrochloride, showing its molecular framework including chlorine atoms and a heterocyclic ring.*

* 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.