Clonidine Hydrochloride Tablet
Product Images NDC 62332-055

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Clonidine Hydrochloride (NDC 62332-055). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Inc., 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

Clonidine 01

Clonidine Hydrochloride Tablets, USP 0.1 mg oral tablets, packaged in a 30-tablet bottle. The label includes NDC 62332-054-30, directions to read accompanying package insert, storage instructions at 25°C with allowed excursions, and a warning to keep out of reach of children. Manufactured by Alembic Pharmaceuticals Inc. in Gujarat, India, with a secondary manufacturing site in New Jersey, USA. The package features a child-resistant closure and the product is Rx only.*

FDA Label Image

Clonidine 02

Label for Clonidine Hydrochloride Tablets USP 0.2 mg by Alembic Pharmaceuticals Inc. The label shows the dosage strength of 0.2 mg with a package count of 30 tablets. It includes storage instructions, warnings such as child resistance, and dosage guidance. The label also features the Alembic logo and barcodes.*

FDA Label Image

Clonidine 03

Label for Clonidine Hydrochloride Tablets, USP 0.3 mg oral tablets by Alembic Pharmaceuticals Inc. The package contains 30 tablets. Labels include dosage and storage directions, a barcode, and the Rx only designation. Manufactured by Alembic Pharmaceuticals Limited and Alembic Pharmaceuticals, Inc. in the USA.*

FDA Label Image

Structure (Clonidine Structure)

Chemical structure of clonidine hydrochloride showing the molecular arrangement including chlorine atoms and the imidazoline 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.