Clonidine Hydrochloride
Product Images NDC 51138-018

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonidine Hydrochloride (NDC 51138-018). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Med-health Pharma, 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

Chemical Structure (Clonidine 01)

Chemical structure of clonidine hydrochloride, showing the molecular arrangement including two chlorine atoms on a phenyl ring connected to an imidazoline ring, complexed as the hydrochloride salt.*

FDA Label Image

Principal Display Panel (0.1 mg Bottle Label)

Label for Clonidine Hydrochloride Tablets, USP 0.1 mg by Med-Health Pharma, LLC. The label states the product contains 30 tablets and is prescription only. Storage instructions indicate controlled room temperature (20-25°C). The label includes manufacturer Mutual Pharmaceutical in Philadelphia and repackager Med-Health Pharma in North Las Vegas, NV. The NDC is 51138-017-30.*

FDA Label Image

Principal Display Panel (0.2 mg Bottle Label)

CLONIDINE HYDROCHLORIDE Tablets, USP 0.2mg label shows a bottle label with 30 tablets, labeled as prescription only. The product is repackaged by Med-Health Pharma, LLC. Storage instructions indicate controlled room temperature (20-25°C). The label also includes the NDC 51138-018-30, manufacturer Mutual Pharmaceutical, and cautions against dispensing without a prescription.*

FDA Label Image

Principal Display Panel (0.3 mg Bottle Label)

Clonidine Hydrochloride Tablets, USP 0.3mg label from Med-Health Pharma, LLC. The label states the product name, strength, dosage form, quantity of 30 tablets, and Rx Only. It includes storage instructions for controlled room temperature (20-25°C), lot and expiration fields, and federal law caution against dispensing without prescription. The label shows the NDC number 51138-019-30 and manufacturer information for Mutual Pharmaceutical, Philadelphia, PA.*

* 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.