Products

HPC-M-FP USP/NF/EP/JP serves various functions in both pharmaceutical and food industries. It acts as a binder, providing cohesion and stability to formulations in both sectors. In pharmaceuticals, it also serves as a controlled release agent, regulating the release of active ingredients over time.

HPC-H-FP USP/NF/EP/JP is a versatile ingredient with multifaceted functions in both pharmaceuticals and food applications. This powder-form substance acts as a binder in both pharma and nutraceutical formulations, ensuring cohesion and integrity. Additionally, it serves as a controlled release agent, enhancing its utility in pharmaceutical applications.

HPC-LM 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.

HICEL™ 25M-USP/NF is a powdered binder designed specifically for pharmaceutical and nutraceutical applications. With water-soluble properties, it ensures ease of use in various pharmaceutical formulations. It serves the pharmaceutical segment, offering reliable binding capabilities to optimize the manufacturing processes of medicinal and nutritional products.

HPC-M-FP USP/NF/EP/JP 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 excipient is available in powdered form and is commonly utilized as a formulation and processing aid in pharmaceutical applications. It is labeled as non-carcinogenic, emphasizing its safety for pharmaceutical formulations. Additionally, it is compliant with TSCA Exempt (USA) and United States Pharmacopeia (USP) standards, ensuring its quality and suitability for pharmaceutical use.

HICEL LP™ 200-USP/NF 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.

HPC L is a powdered excipient primarily composed of hydroxypropyl cellulose. It complies with various regulatory standards. This excipient is water-soluble and is commonly used in the formulation and processing of pharmaceuticals. It falls under the category of formulation and processing aids within the excipients product family in the pharmaceutical and nutraceutical technology sector. Additionally, it carries the labeling claim of being non-carcinogenic.

HICEL™ SMCC 90M is a white to off-white colored powder, this substance is co-processed microcrystalline cellulose with colloidal silicon dioxide.

HILOSE™ USP, known by its chemical name croscarmellose sodium, is a solid disintegrant provided in powdered form. It is a crucial component in pharmaceutical manufacturing, functioning as a disintegrant to facilitate the breakdown of tablets and improve their dissolution. Categorized under binders and disintegrants in the healthcare and pharmaceutical market, it plays a vital role in ensuring the effectiveness of pharmaceutical formulations.

HPC-H-FP USP/NF/EP/JP have multifaceted functions in both pharmaceuticals and food applications. This powder-form substance acts as a binder in both pharma and nutraceutical formulations, ensuring cohesion and integrity. Additionally, it serves as a controlled release agent, enhancing its utility in pharmaceutical applications.

HPC-L-FP USP/NF/EP/JP is an excipient primarily composed of hydroxypropylcellulose. It meets regulatory standards, including the European Pharmacopeia (Ph. Eur.), Japan Pharmacopeia (JP), and National Formulary (NF). It is also compliant with the United States Pharmacopeia (USP) and is TSCA Exempt (USA) certified. This water-soluble excipient, available in powdered form, is commonly used in pharmaceutical applications as a formulation and processing aid. It carries the labeling claim of being non-carcinogenic, underscoring its safety for use in pharmaceutical formulations.

HICEL™ 12-USP/NF 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.

HICEL™ 50M-USP/NF 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.

CELNY-L-FP2 is a powdered excipient primarily composed of hydroxypropyl cellulose. It complies with regulatory standards, including being FCC (Food Chemicals Codex) compliant and meeting the specifications outlined in the Japan Pharmacopeia. This product is available in powder form and falls under the category of Other excipients within the excipients product family in the pharmaceuticals and nutraceuticals technology sector.

HPC-M USP/NF/EP/JP 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, assuring its quality and suitability for pharmaceutical applications.