Dextrin

Pharmaceutical Dextrin—also known as pharmaceutical-grade dextrin (CAS No. 9004-53-9)—is a polysaccharide-based pharmaceutical excipient refined from natural starch through a process involving heating and acid hydrolysis modification, in strict compliance with national pharmacopoeia standards. It serves as an indispensable foundational excipient within the pharmaceutical industry. Its quality strictly adheres to current pharmacopoeia specifications, such as CP2020 and USP; furthermore, having successfully completed CDE Class A registration and filing, it fully satisfies the regulatory compliance requirements for pharmaceutical formulation manufacturing.
This product presents as a white or off-white amorphous powder with a loose, fine texture. It is odorless, free of impurities, and exhibits stable physicochemical properties. The product boasts excellent solubility, dissolving rapidly in boiling water while remaining insoluble in organic solvents such as ethanol and diethyl ether. Possessing superior binding, molding, and stability characteristics, it is well-suited to meet the manufacturing and processing demands of various pharmaceutical formulations. Its strong compatibility ensures it does not readily react with active pharmaceutical ingredients (APIs), thereby effectively safeguarding the quality and stability of the finished medication.
In pharmaceutical applications, dextrin serves a wide range of purposes; primarily, it functions as a filler, binder, and thickener for tablets, capsules, and granules, while also acting as an emulsifying stabilizer and molding aid. When utilized in the production of solid dosage forms, it effectively enhances the molding properties of the medicinal powder, improves tablet hardness and surface smoothness, and optimizes the disintegration and dissolution profiles of the formulation. Additionally, it boosts the stability of active ingredients, preventing moisture absorption, caking, and degradation of the medication, thereby significantly increasing the pass rate of the finished pharmaceutical products.
The product is manufactured in GMP-standardized workshops under comprehensive,全程 quality control. For every production batch, a complete set of documentation—including detailed quality inspection reports and regulatory filing credentials—is provided. The standard packaging consists of 25kg sealed bags, designed to be moisture-proof and light-shielding for convenient storage and transport. We support bulk orders and customized packaging options. Widely applicable across various pharmaceutical settings—including pharmaceutical manufacturers, formulation plants, and medical research institutions—this product stands as a highly cost-effective and fully compliant pharmaceutical excipient.