Mineral active ingredients and excipients for pharmaceutical application
Talk to our pharma expertsMAGNESIA is your specialised partner for mineral raw materials in the pharmaceutical industry.
For over four decades, we have been supplying manufacturers and developers with verified active ingredients and excipients that meet the requirements of international pharmacopoeias. Our products are used in solid, semi-solid and liquid dosage forms – from tablets and capsules to suspensions and infusion solutions.
As a GDP-certified active substance distributor with comprehensive quality management, we supply not only raw materials but also regulatory assurance and technical consultancy – reliable, documented and individual.

Diverse application areas in pharmaceutical formulations
Our mineral compounds are suitable for a wide range of pharmaceutical applications. They meet functional requirements such as flow behaviour, compressibility or solubility while also being verified for regulatory compliance. Whether you are optimising an established product or developing a new formulation – we support you with suitable raw materials and comprehensive documentation.
- Tablets, coated tablets, capsules
- Powders & granules
- Suspensions, solutions, infusions
- Ointments, creams, lotions
- Effervescent tablets, lozenges, suppositories
- Products for enteral nutrition
Mineral raw materials for the pharmaceutical industry
Our portfolio comprises over 100 mineral compounds that can be used as active ingredients and excipients. The products are available in various qualities, particle sizes and bulk densities and meet the requirements of relevant pharmacopoeias.
Magnesium compounds
Inorganic:
- Magnesium carbonate
- Magnesium oxide
- Magnesium chloride
- Magnesium phosphate
- Magnesium hydroxide
- Magnesium sulfate
Organic:
- Magnesium ascorbate
- Magnesium lactate
- Magnesium aspartate
- Magnesium malate
- Magnesium citrate
- Magnesium pidolate
- Magnesium gluconate
- Magnesium taurate
- Magnesium glycerophosphate
- Magnesium stearate
Calcium compounds
Inorganic:
- Calcium carbonate
- Calcium oxide
- Calcium chloride
- Calcium phosphate
- Calcium hydroxide
- Calcium sulfate
Organic:
- Calcium citrate
- Calcium lactate
- Calcium gluconate
- Calcium glycerophosphate
- Calcium stearate
- Lithothamniumcalcerum
Potassium compounds
- Potassium carbonate
- Potassium citrate
- Potassium bicarbonate
- Potassium phosphate
- Potassium chloride
- Potassium stearate
Sodium compounds
- Potassium ascorbate
- Potassium chloride
- Potassium bicarbonate
- Potassium citrate
- Potassium carbonate
- Potassium sulfate
MagGran® | DC grades
- Direct pressable variants of magnesium and calcium compounds
MagChel® | Chelates
- Calcium bisglycinate
- Magnesium bisglycinate
- Copper bisglycinate
- Manganese bisglycinate
- Iron bisglycinate
- Zinc bisglycinate
Zinc compounds
- Zinc oxide
- Zinc gluconate
- Zinc citrate
- Zinc acetate
- Zinc stearate
Manganese compounds
- Manganese bisglycinate
- Manganese gluconate
- Manganese citrate
- Manganese glycerophosphate
Vitamins
- RiviK2 (Vitamin K2 in trans-MK‑7 form, oil- or powder-based)
- Nutra‑C (Vitamin C)
- Vitamin B5
Mineral raw materials for the pharmaceutical industry
MAGNESIA offers a specialised range of mineral raw materials for the pharmaceutical industry – qualified, documented and ready for use in medicinal products. Our products meet the requirements of international pharmacopoeias and are suitable for a wide variety of dosage forms.
With technical consultancy, regulatory expertise and comprehensive documentation, we support you in the safe and efficient realisation of your pharmaceutical product ideas.
High standards for pharmaceutical raw materials
Our mineral raw materials come from qualified manufacturers and meet the requirements of international standards. Purity, traceability and regulatory compliance are at the centre of our quality assurance – regardless of the area of application.
Manufacturers worldwide trust our expertise and our consistent orientation towards applicable standards. Our processes are documented, verified and aligned with the requirements of the pharmaceutical industry.
- German Medicinal Products Act (AMG) and Ordinance on the Manufacture of Medicinal Products and Active Pharmaceutical Ingredients (AMWHV)
- International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
- IPEC Europe
- European Directorate for the Quality of Medicines & HealthCare (EDQM)
- European Medicines Agency (EMA)




