ZMC Upgrades Vitamin E Facility

September 8, 2010

1 Min Read
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THE WOODLANDS, TexasZhejiang Medicine Company / Xinchang Pharmaceutical Co. Ltd. (ZMC) upgraded its dl alpha tocopheryl acetate manufacturing facility.

The completed upgrades to this manufacturing facility are resulting in a 98-percent plus assay product with consistently lower impurities, less color and more favorable viscosity than existing synthetic vitamin E products," said Chunbo Li, chairman, ZMC. 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." He 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."

Zhejiang Medicine Company (ZMC) is an active ingredient manufacturer offering high-quality pharmaceutical and nutraceutical ingredients worldwide since 1954. ZMC is staffed with more than 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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