Clonidine Hydrochloride
Product Images NDC 51138-017
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 51138-017). 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.
Principal Display Panel (0.1 mg Bottle Label)
This is a description of Clonidine Hydrochloride Tablets. The text contains information about the manufacturer, dosage, and storage instructions. It also includes a caution regarding dispensing without a prescription. The tablets are available in 0.1mg strength and come in a package of 30 tablets. The text provides the contact information for the repackaged company as well. The lot number of the tablets is included as well.*
Principal Display Panel (0.2 mg Bottle Label)
This product is Clonidine Hydrochloride tablets, a medication used for the treatment of high blood pressure. The tablets come in a container with 20 tablets, each containing 0.2mg of the active ingredient. It is manufactured by Mutual Pharmaceutical and packaged by Med Health Pharma. The package insert should be consulted for full prescribing information, and it is important to note that dispensing without a prescription is prohibited by law. Storage should be at a controlled room temperature of 20-25 degrees Celsius (68-77 degrees Fahrenheit).*
Principal Display Panel (0.3 mg Bottle Label)
Clonidine Hydrochloride Tablets, USP with a strength of 0.3mg and packed in 30 tablets per pack. It is manufactured by Mutual Pharmaceutical located in Philadelphia, PA and repackaged by Med-Health Pharma in North Las Vegas, NV. The product should be stored at a controlled room temperature of 20-25°C (68-77°F). The dosage information is provided in the package insert. The NDC number of the product is 51138-019-30. This is a prescription-only medication and requires federal law compliance. The other values are not available to read.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.