Products

ACECEL® 101-USP/NF is a white or almost white, Fine or granular powder. It consists of free flowing, non fibrous particles. It has high-quality microcrystalline cellulose powder designed for pharmaceutical applications. Microcrystalline cellulose is a widely used excipient in the pharmaceutical industry, known for its excellent binding, disintegration, and flow properties. This product is a trusted and compliant choice when seeking microcrystalline cellulose for their drug formulations.

ACECEL® 102-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 versatile compound can be confirmed as it turns violet-blue when in contact with an iodinated zinc chloride solution.

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.

AMBER PET, USP utilized as a lubricant, plays a pivotal role in pharmaceutical manufacturing within the healthcare and pharma industry.

AMMONIUM SULFATE NF GR2033 is in solid form and is designated for the healthcare and pharmaceutical markets, with specific applications in API (active pharmaceutical ingredient) manufacturing.

CAMPHOR (USP) SYNTHETIC 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).

CAP CAPRYLIC TRI-E6000-RSPO MB is a high-quality product compliant with various pharmaceutical standards. This versatile product serves as both an emollient and a solvent, making it suitable for a range of pharmaceutical and nutraceutical applications, especially as a base fluid, glidant, or lubricant in various formulations.

CAP CAPRYLIC TRI-E6000-RSPO MB is a high-quality product compliant with various pharmaceutical standards. This versatile product serves as both an emollient and a solvent, making it suitable for a range of pharmaceutical and nutraceutical applications, especially as a base fluid, glidant, or lubricant in various formulations.

CAPRIC CAPRYLIC TRIGLYC-E6000 is a liquid emollient and solvent that complies with various pharmacopeias. This versatile product serves as an emollient and solvent in pharmaceutical and nutraceutical applications, adhering to the National Formulary (NF) standards to ensure quality and suitability for various uses.

CAPRIC CAPRYLIC TRIGLYC-E6000 is a liquid emollient and solvent that complies with various pharmacopeias. This versatile product serves as an emollient and solvent in pharmaceutical and nutraceutical applications, adhering to the National Formulary (NF) standards to ensure quality and suitability for various uses.

CAPRIC CAPRYLIC TRIGLYC.-E6300 is a liquid emollient and solvent that adheres to stringent regulatory and compliance standards. This product serves as an emollient and solvent, meeting the standards outlined in the National Formulary (NF) for pharmaceutical and nutraceutical applications.

CAPRIC CAPRYLIC TRIGLYC.-E6300 is a liquid emollient and solvent that adheres to stringent regulatory and compliance standards. This product serves as an emollient and solvent, meeting the standards outlined in the National Formulary (NF) for pharmaceutical and nutraceutical applications.

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.

CHLORPHENIRAMINE MALEATE USP is an active pharmaceutical ingredient (API) that serves a crucial role in the pharmaceutical and nutraceutical industry. Its primary function lies in its anti-histamine properties, making it effective in alleviating allergy symptoms and related conditions. Chemically, it is known as Chlorpheniramine Maleate and is available in a powdered physical form. This product complies with quality and safety standards set by the United States Pharmacopeia (USP), ensuring its suitability for pharmaceutical formulations and use in various medications.

COMPRESSUC MS 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. This product is very soluble in water.