Clonidine Hydrochloride Tablet
Product Images NDC 52817-183

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Clonidine Hydrochloride (NDC 52817-183). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trupharma, 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

The Structural Formula For Clonidine Hydrochloride Is An Imidazoline Derivative And Exists As A Mesomeric Compound. The Chemical Name Is 2-(2,6-dichlorophenylamino)-2-imidazoline Hydrochloride. (Clonidine Hydrochloride 01)

Chemical structure diagram of Clonidine hydrochloride, showing the molecular arrangement including a dichlorophenyl ring and an imidazoline ring, associated with hydrochloride (HCl).*

FDA Label Image

Principal Display Panelndc 52817-180-10clonidinehydrochloridetablets, Usp0.1 mgrx Only100 Tablets (Clonidine Hydrochloride 02)

Clonidine Hydrochloride Tablets, USP 0.1 mg oral tablet label showing a package of 100 tablets. The label includes the NDC number 52817-180-10 and states the manufacturer is Frontida BioPharm, Inc., with distribution by TruPharma, LLC. It includes storage instructions, tablet identification as MP 657, and a barcode.*

FDA Label Image

Principal Display Panelndc 52817-180-00clonidinehydrochloridetablets, Usp0.1 mgrx Only1000 Tablets (Clonidine Hydrochloride 03)

Label for Clonidine Hydrochloride Tablets, USP 0.1 mg, showing the drug name and strength prominently on an orange background. The label states the quantity as 1000 tablets, prescription only, and includes storage instructions, tablet debossing details (MP 657), manufacturer Frontida BioPharm, Inc., and distributor TruPharma, LLC. Barcode and revision date 07/17 are also visible.*

FDA Label Image

Principal Display Panelndc 52817-181-10clonidinehydrochloridetablets, Usp0.2 mgrx Only100 Tablets (Clonidine Hydrochloride 04)

Label for Clonidine Hydrochloride Tablets, USP 0.2 mg by TruPharma, LLC. The label shows the NDC 52817-181-10 and states each tablet contains 0.2 mg clonidine hydrochloride USP. It includes storage instructions and manufacturer details from Frontida BioPharm, Inc. The package contains 100 tablets and is marked Rx only.*

FDA Label Image

Principal Display Panelndc 52817-181-00clonidinehydrochloridetablets, Usp0.2 mgrx Only1000 Tablets (Clonidine Hydrochloride 05)

Label for Clonidine Hydrochloride Tablets, USP 0.2 mg oral tablets. The label shows the NDC 52817-181-00, indicates a quantity of 1000 tablets, and states Rx Only. Manufactured by Frontida BioPharm, Inc. and distributed by TruPharma, LLC. Storage instructions and dispensing details are also included.*

FDA Label Image

Principal Display Panelndc 52817-182-10clonidinehydrochloridetablets, Usp0.3 mgrx Only100 Tablets (Clonidine Hydrochloride 06)

Label for Clonidine Hydrochloride Tablets USP 0.3 mg, oral tablets. The label shows the product name and strength prominently in white text on a teal background, with 100 tablets count and 'Rx Only.' It includes the NDC number 52817-182-10, manufacturer Frontida BioPharm, Inc., and distributor TruPharma, LLC. Storage instructions and dispensing warnings are also visible.*

FDA Label Image

Principal Display Panelndc 52817-182-00clonidinehydrochloridetablets, Usp0.3 mgrx Only1000 Tablets (Clonidine Hydrochloride 07)

Label for Clonidine Hydrochloride Tablets USP 0.3 mg, oral tablets in a package of 1000 tablets. Manufactured by Frontida BioPharm, Inc. and distributed by TruPharma, LLC. The label includes storage instructions, tablet debossing (MP 659), NDC code 52817-182-00, and a barcode.*

* 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.