ZMC Completes Vitamin E Plant Upgrade

Zhejiang Medicine Company / Xinchang Pharmaceutical Co. Ltd. (ZMC) have announced the completion of the upgrade to its dl alpha tocopheryl acetate manufacturing facility. Chunbo Li, Chairman, ZMC, stated “the completed upgrades to this manufacturing facility are resulting in a 98%+ assay product with consistently lower impurities, less color and more favorable viscosity than existing synthetic Vitamin E products.” Mr. Li further commented “The upgraded operation has been constructed to address the growing attention to environmentally responsible manufacturing incorporating state of the art self-contained air and waste water treatment facilities.”

Sander Krupski. National Sales Manager, ZMC-USA, reiterated “ZMC dl alpha tocopheryl acetate joins the growing list of products considered as superior quality and high value as produced by our parent company, ZMC. ZMC-USA stands ready for the opportunity to provide direct from the manufacturer representation for this product manufactured in one of the most ecologically state of the art synthetic Vitamin E plants.” Mr. Krupski added “ZMC-USA offers the only USP Ingredient Verified dl alpha tocopheryl acetate. This important third party endorsement assures the process as well as the product has been thoroughly audited to assure the highest quality and safety.”

ABOUT: Zhejiang Medicine Company (ZMC) is an active ingredient manufacturer offering high quality leading edge pharmaceutical and nutraceutical ingredients worldwide since 1954. ZMC is staffed with over 4,000 employees globally and is an important production base of pharmaceutical drugs, Biotin, Vitamin A, Astaxanthin, Natural and Synthetic Vitamin E, Patented Lutein, Phytosterol, B-Carotene, Zeaxanthin, Lycopene, and Coenzyme Q10. ZMC operates in North America as ZMC-USA from its office in The Woodlands, Texas.

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