Products

This product, utilized as a lubricant, plays a pivotal role in pharmaceutical manufacturing within the healthcare and pharma industry.

This product is a blend of esters, combining stearic acid with glycol and polyethylene glycol. This product presents as a creamy, white to cream-colored substance with a subtle fragrance. This product offers an effective solution for formulators seeking a versatile ingredient with desirable tactile qualities and ease of use.

This product is a pharmaceutical-grade crystalline glucose monohydrate, also known as dextrose. It is suitable for both human and veterinary use as an excipient. This product conforms to the current Ph. Eur. and USP-NF standards for glucose monohydrate and dextrose. It is produced through the crystallization of glucose syrup obtained from the hydrolysis of edible starch.

This product is a valuable component in pharmaceutical manufacturing, serving as efficient capsules. These solid capsules play a crucial role in various applications, especially in pharmaceutical manufacturing, where excipients and coatings are essential. They comply with TSCA Exempt (USA) regulations, ensuring their suitability for use in pharmaceutical and nutraceutical formulations.

This ingredient, known as Sodium Carbonate Monohydrate, is a source of the mineral sodium. It functions as a mineral source and supplement in food ingredients, as well as in pharma & nutraceuticals as a dietary supplement and mineral source. It comes with features that make it suitable for various dietary preferences, such as being free of major allergens, hygroscopic, non-irradiated, odorless, and suitable for both vegans and vegetarian foods.

This product is designed for pharmaceutical and nutraceutical purposes, are efficiently packaged in cartons, and possess FDA approval. With halal and kosher certifications, they accommodate diverse dietary requirements. Furthermore, they adhere to the National Formulary (NF) standards, TSCA (USA) guidelines, and USP requirements, making them ideal for applications involving modified and controlled release in the pharmaceutical and nutraceutical sectors.

This product is primarily used in the pharmaceutical and nutraceutical industries. They serve as capsules for delivering various types of medications and supplements. These capsules can be used for modified and controlled release formulations, making them suitable for applications that require specific dosing schedules or the gradual release of active ingredients.

This product is a fine, white, or almost white powder obtained from the tuber of Solanum tuberosum L. This potato starch is labeled as non-GMO, allergen-free, halal, and Kosher. It complies with the European Pharmacopeia (Ph. Eur.) standards and is used in pharmaceuticals and nutraceuticals as an excipient.

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

In powder form, it functions as a buffering agent in pharmaceuticals and nutraceuticals.

This product is a solid powder pharmaceutical ingredient primarily used as a polishing agent for tablets. It finds application in the pharmaceutical industry, particularly in drug delivery and care solutions for oral dosage forms.

This product is an excipient primarily composed of Hydroxypropylcellulose. It complies with various regulatory standards, including the European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia, and National Formulary (NF). This excipient is available in both powdered and solid forms and is utilized in various pharmaceutical applications. Additionally, it meets the standards of the United States Pharmacopeia (USP), ensuring its quality and suitability for pharmaceutical use.

This product is primarily used in the pharmaceutical and nutraceutical industries. The key ingredient in these capsules is hypromellose, also known as HPMC (hydroxypropyl methylcellulose). They are classified as excipients, specifically for modified and controlled-release applications in pharmaceuticals and nutraceuticals.

This product is a powdered excipient primarily composed of Hydroxypropylcellulose. It conforms to several regulatory standards, including the European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia (JP), National Formulary (NF), and it is TSCA Exempt (USA) and United States Pharmacopeia (USP) compliant. This excipient is water-soluble and is widely utilized in pharmaceutical applications, particularly as a formulation and processing aid. Notably, it carries the labeling claim of being non-carcinogenic, making it a safe choice for pharmaceutical formulations.

This product provides an exceptionally low lead content, making it suitable for applications where the strictest lead requirements must be met. This API version is manufactured in an FDA registered drug establishment facility that has undergone FDA inspections for compliance with ICH-Q7 GMP for API. It also meets 21CFR111 GMP standards for Dietary Supplements (DS).