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Zeta has a long history of importing bulk active and inactive
ingredients for the US market. In past years this included
nutritionals. Since 2001, our emphasis has been OTC and prescription
pharmaceutical markets. As a result, we offer a broad and more
diversified range of APIs to human and veterinary dosage
manufacturers.
Over the years our focus has been to offer a lower cost alternative
to our customer’s existing sources. With this charter comes the
responsibility to present manufacturers who meet cGMP and FDA
standards. To facilitate this process we continue to retain the
services of FDA consultants to monitor GMP submissions and to
conduct pre-FDA inspections.
A number of our products are schedule III and IV controlled
substances. We are most familiar with the regulatory guidelines and
have the necessary DEA permits and warehouse facilities to handle
these products.
Our list of products continues to expand. Our multi-lingual staff
and combined years of experience makes Zeta Pharmaceuticals a
resourceful partner. We welcome the opportunity to earn a position
as one of your suppliers.
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