Samarin® is manufactured with pharma-grade raw material from active extracts of European Milk Thistle, formulated into tablet for fast dissolving and high bioavailability.

It is manufactured as a pharmaceutical product at a GMP pharmaceutical plant with the same rigorous standards as for other pharmaceutical products at the plant.*

Active compounds of Silymarin are highly insoluble, and they must be formulated to make them bioavailable. Solubility varies based on manufacturing technology. Samarin® solubility and other quality measures complies with the latest standards in the US Pharmacopoeia (USP 38). *

Does your Silymarin/Milk Thistle product meet US Pharmacopoiea standards?


Solubility and bioavailability are critical to product efficacy.

Check if your product meets the latest U.S. standards.

Check if the quality was measured with the advanced and reliable-HPLC-tested method

Samarin® is.

‡These statements have not been evaluated by the US FDA

* Product statements have not been approved by the US FDA. The product is not intended to treat, cure or prevent disease.

DISCLAIMER: The information offered should not be construed as medical advice; please consult your doctor before taking Silymarin, and nothing you have read here should cause you to delay seeking medical advice.


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