Other Pharmaceutical Manufacturing Applications

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 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 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.

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.

It is available as pellets and serves as a controlled-release agent in pharmaceutical and nutraceutical contexts. It consists of an 80% blend of dibasic calcium phosphate anhydrous and 20% microcrystalline cellulose.

This is an active pharmaceutical ingredient (API) with a specific functionality in the pharmaceutical and nutraceutical industries. Its primary function is as an antihistamine, making it valuable for addressing allergic reactions and related conditions. This product is available in a powdered physical form, characterized by its water solubility, appearing as a white odorless crystalline powder. One of its notable features and benefits is that it is non-carcinogenic, ensuring safety in pharmaceutical formulations.

This product is a high-quality ingredient known for its solubility in alcohol. This product consists of melatonin, a widely recognized compound. Melatonin, found in both solid and powder forms, serves as a valuable dietary supplement in the pharmaceutical and nutraceutical sectors. It complies with the standards of the United States Pharmacopeia (USP), ensuring its quality and suitability for a range of dietary supplement formulations.

It is meticulously formulated to meet the exacting standards of the healthcare and pharmaceutical industry, specifically tailored for drug delivery and care solutions in oral applications.

This product is identified by its chemical name Camphor, is a regulatory-compliant product. This synthetic camphor is available in the form of crystals. It is noteworthy that this product is non-carcinogenic and exempt from TSCA regulations in the USA, meeting the standards of the United States Pharmacopeia (USP).

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.

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.