Products

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.

GRANULAC® 70 is lactose, a water-soluble powder used in the manufacturing of capsules for oral drug delivery and care solutions in the healthcare and pharmaceutical industries. It complies with various certifications and standards, including Kosher, Halal, and pharmacopeias such as USP and Ph. Eur.

MALDEX 190 PHARMA 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.

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.

MALDEX G 120 PHARMA is meticulously crafted to meet the exacting standards of the healthcare and pharmaceutical industries, specifically designed for oral drug delivery and care solutions. Available in both granules and powder forms, ensures versatile application and ease of formulation.

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.

HPC-SSL 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 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.

HICEL™ 90M-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.

MALDEX 190 PHARMA 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.

ACECEL® 200-USP/NF is a fine or granular powder with a white or almost white appearance. It is composed of free-flowing, non-fibrous particles. It exhibits the following solubility properties: it is practically insoluble in sodium hydroxide solution (1 in 20) and insoluble in water, dilute acids, and most organic solvents. Identification of this product can be confirmed as it turns violet-blue when in contact with iodinated zinc chloride solution.

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.

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.