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27 February 1997

Johnson Matthey Receives Important New Product Manufacturing Approvals

Johnson Matthey's Biomedical Materials business has received manufacturing registrations from the US Drug Enforcement Administration (DEA) for a broad range of controlled drug active ingredients and raw materials. These products include dihydrocodeine, diphenoxylate, hydrocodone, levorphanol, methadone, oxycodone, oxymorphone and thebaine. They are used in a range of pharmaceutical applications, primarily in pain management. There are well established markets for these materials in the US, which include many generic drug manufacturers. The total available US market for these products is worth approximately $ 70 million per annum.

Commenting on the DEA registrations, Dr Mike Cleare, Managing Director with responsibility for the Biomedical Materials business, said:

"Pharmaceutical Materials represent an important growth opportunity for Johnson Matthey. We expect that the development and commercialisation of new products such as these, along with our strong technical capabilities and commitment to customer service, will continue to drive the rapid expansion of the important controlled substances segment of our business."

Johnson Matthey's Biomedical Materials business, located in West Deptford, New Jersey, USA, manufactures and markets a broad range of active pharmaceutical ingredients including methylphenidate, fentanyl and other controlled drug products as well as the important anti-cancer drugs, cisplatin and carboplatin.

Enquiries:
Johnson Matthey
Ian Godwin
Group Public Relations Manager
+44 (0)171 269 8410