Pharmaceutical Manufacturing

This product is a U.S. Pharmacopeia and Food Chemicals Codex (FCC)-compliant calcium carbonate presented as a fine, white to off-white microcrystalline powder. It is produced by purifying naturally occurring limestone sourced from the Western United States. Carbonates like This product meet the requirements for use in the formulation of dietary supplements and drugs in accordance with U.S. Food and Drug Administration regulations.

It contains sucrose (from beet) C12H22O11 (95-98% on a dry basis), maltodextrin (from maize), and invert sugar syrup (from beet). It is a practically white, crystalline, odorless powder with a sweet taste. It is very soluble in water.

This product is a white, crystalline powder with a slightly alkaline taste and insolubility in alcohol, is primarily utilized in the food, personal care, home care, and pharmaceutical industries for excipient purposes. It is intended for further manufacturing, reprocessing, and repackaging, specifically not for use in hemodialysis or as an active pharmaceutical ingredient.

This product is a clear, water-white, hygroscopic liquid with a mild ammoniacal odor. It finds versatile applications across various industries, serving as a key chemical intermediate in the production of cosmetics, surface-active agents, emulsifiers, pharmaceuticals, plasticizing agents, gas-scrubbing in refining and natural gas processes, and in the manufacturing of carbon dioxide and ammonia.

This product is primarily composed of glycerin and serves as a valuable ingredient in various applications. This product is naturally derived and sourced from natural, plant-based, and vegetable origins, meeting the demand for naturally sourced ingredients. It complies with the United States Pharmacopeia (USP) standards, ensuring its quality and suitability for various applications. It is widely used in pharmaceutical manufacturing, specifically for other pharmaceutical manufacturing applications.

It is presented as pellets and functions as a controlled-release agent in pharmaceutical and nutraceutical applications. It contains a mixture of 80% dibasic calcium phosphate anhydrous and 20% microcrystalline cellulose.

This ingredient is a source of the mineral sodium. It functions as a mineral source and supplement in both food ingredients and pharma & nutraceuticals applications, contributing to dietary needs and supplement formulations.

This product is an excipient primarily composed of Hydroxypropylcellulose. It conforms to regulatory standards, including the European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia, and National Formulary (NF). This product is available in both powdered and solid forms, serving as an excipient. Furthermore, it is compliant with the United States Pharmacopeia (USP) standards, providing assurance of its quality and suitability for pharmaceutical applications.

This product is an excipient primarily composed of Hydroxypropylcellulose. It adheres to various regulatory standards, including the European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia (JP), and National Formulary (NF). This product is available in both powdered and solid forms and is commonly used as an excipient in pharmaceutical applications. Furthermore, it is compliant with the United States Pharmacopeia (USP) standards, ensuring its quality and suitability for pharmaceutical use.

This product is an excipient primarily composed of Hydroxypropylcellulose. It complies with various regulatory standards, including the European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia (JP), and National Formulary (NF). Additionally, it is certified as TSCA Exempt (USA) and United States Pharmacopeia (USP) compliant. This water-soluble excipient is available in powdered form and is commonly used in pharmaceutical applications as a formulation and processing aid. It carries the labeling claim of being non-carcinogenic, ensuring its safety for use in pharmaceutical formulations.

This product is a white or almost white powder composed of free-flowing, non-fibrous particles. It is practically insoluble in sodium hydroxide solution (1 in 20) and exhibits insolubility in water, dilute acids, and most organic solvents. When exposed to an iodinated zinc chloride solution, this substance turns violet-blue.

It is meticulously crafted to meet the exacting standards of the healthcare and pharmaceutical industry, specifically tailored for oral drug delivery and care solutions. Utilizing advanced manufacturing technologies including wet granulation, spray drying, and dry granulation, our granules ensure optimal performance and efficacy.

This product is a versatile pharmaceutical and nutraceutical ingredient with several key advantages. It is allergen-free, ensuring its suitability for a wide range of consumers. This product is available in convenient bag packaging. Additionally, This product is GMO-free, making it a preferred choice for health-conscious consumers. It is also certified as Halal and Kosher, catering to specific dietary requirements. It is recognized by the United States Pharmacopeia (USP) and is suitable for both vegan and vegetarian diets, contributing to its broad applicability in pharmaceutical and nutraceutical formulations.

It is in pellet form and acts as a controlled-release agent for pharmaceutical and nutraceutical applications. It comprises an 80% blend of dibasic calcium phosphate anhydrous and 20% microcrystalline cellulose.

This product is a liquid pharmaceutical ingredient that meets high regulatory and compliance standards, ensuring its quality and suitability for pharmaceutical manufacturing applications. It offers a versatile solution for formulators seeking to meet the strict standards and quality requirements of the healthcare and pharmaceutical industry.