Active Pharmaceutical Ingredients (APIs)

MERIDEX PF is crafted to meet the stringent requirements of the healthcare and pharmaceutical industries, particularly in APIs and pharmaceutical formulations. This water-soluble powder serves multiple functions, including acting as a sweetener, parenteral nutrient, and API intermediate.

OMYA-CAL USP-4-AZ is primarily composed of calcium carbonate. It meets several regulatory and compliance standards, including FCC Compliance, FSSC 22000, Halal, ISO 14001, ISO 9001, and Kosher. This mineral has various applications in the food and nutrition industry, particularly in nutraceuticals and supplements. It is certified as non-carcinogenic and follows OHSAS standards. The product is available in powdered form and may include silica as an additional component. It is also exempt from TSCA (Toxic Substances Control Act) regulations in the USA. Additionally, it is relevant in the pharmaceutical and nutraceutical sectors as a mineral supplement.

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.

DIPHENHYDRAMINE HCL USP KONGO 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.

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).

FUROSEMIDE USP is a white to slightly yellow, odorless crystalline powder used as an active pharmaceutical ingredient (API). It serves as an antihypertensive and diuretic in pharmaceutical and nutraceutical applications. The powder is soluble in various solvents but insoluble in water.

OMYA-CAL USP-15-AZ consists mainly of calcium carbonate, serving as its primary ingredient. It complies with several regulatory standards and certifications, including FCC Compliance, FSSC 22000, Halal, ISO 14001, ISO 9001, and Kosher. This mineral is used in various applications within the food and nutrition industry, particularly in nutraceuticals and supplements. It is also certified as non-carcinogenic and complies with OHSAS standards. This product is available in powdered form and may contain silica as an additional component. Additionally, it is exempt from TSCA (Toxic Substances Control Act) regulations in the USA. It is also relevant in the pharmaceutical and nutraceutical sectors as a mineral supplement.

Sodium Chloride Sanal P is a pharmaceutical-grade sodium chloride product designed for dialysis APIs. This water-soluble salt is suitable for use in injectable pharmaceutical and nutraceutical applications, characterized by its non-carcinogenic nature and odorless properties. This product is the trusted choice for pharmaceutical and nutraceutical formulations, ensuring high quality and safety standards in dialysis APIs and injectable dosage forms.

MERIDEX is meticulously crafted to meet the stringent requirements of the healthcare and pharmaceutical industries, particularly in parenteral applications. This water-soluble powder is essential for various pharmaceutical formulations, ensuring high quality and compliance with international standards.

SODIUM BICARB USP #1 PWD is a white, slightly alkaline crystalline powder that is insoluble in alcohol and is primarily employed in the food, personal care, and home care industries, often as an excipient in pharmaceuticals. It is intended for further manufacturing, reprocessing, and repackaging, with strict avoidance of use in hemodialysis or as an active pharmaceutical ingredient.