Sodium Bicarbonate USP Grade - Pharmaceutical Excipient & Food Additive Supplier

As a supplier of USP Grade Sodium Bicarbonate, our product strictly complies with the monograph specifications of the United States Pharmacopeia, a quality benchmark widely recognized by global pharmaceutical regulatory systems. The USP grade signifies that the product not only meets chemical purity standards but also satisfies the stringent safety requirements for parenteral or oral dosage forms regarding microbial load, endotoxins (for injectable grade), insoluble matter, and limits for specific related substances (e.g., sodium carbonate, chloride, sulfate). In the pharmaceutical industry, sodium bicarbonate plays a dual role. Primarily, as an Active Pharmaceutical Ingredient (API), it is the core of antacids and drugs for correcting acidosis. Secondly, as an excipient, its functions are diverse and critical. In direct compression or dry granulation processes, its inherent compressibility and diluent properties allow it to function as a filler or diluent. Due to its ability to rapidly generate carbon dioxide gas upon contact with water or gastric acid, it is widely used as a disintegrant and gas-generating agent in effervescent tablets and fast-dissolving tablets, significantly enhancing drug dissolution rate and bioavailability, and improving patient compliance. Examples include Vitamin C effervescent tablets and Aspirin effervescent tablets, which rely on its gas-producing action. Concurrently, in the food additive sector, achieving USP-grade quality enables its seamless integration into high-end health products, functional foods, and food manufacturing with stringent requirements for raw material traceability and quality control. It can be used to produce effervescent nutritional supplements (e.g., calcium-magnesium effervescent tablets, multivitamin effervescent tablets), offering convenient dosage forms while ensuring the stability and activity of active ingredients. Our production system is managed under cGMP (current Good Manufacturing Practice) principles, implementing rigorous controls and complete documentation from raw material procurement through manufacturing to product release. This ensures product consistency and traceability, meeting the ultimate expectations of the pharmaceutical and high-end food industries for supply chain transparency and quality reliability.