Abraxis Bioscience (MM) (NASDAQ:ABBI)
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From Mar 2020 to Mar 2025

Abraxis BioScience, Inc. (NASDAQ:ABBI), an integrated, global
biopharmaceutical company, today announced final approval from the U.S.
Food and Drug Administration (FDA) for its Abbreviated New Drug
Application (ANDA) for Fosphenytoin Sodium Injection, 100 mg, 2 mL and
500 mg, 10 mL vials, USP, the generic equivalent of Pfizer�s
Cerebyx�. According
to IMS, sales in 2006 of fosphenytoin sodium injection in the United
States exceeded $73 million. The company expects to commence marketing
of fosphenytoin sodium injection in August 2007. The product is AP
rated, preservative-free and latex-free.
Fosphenytoin Sodium Injection is indicated for short-term parenteral
administration when other means of phenytoin administration are
unavailable, inappropriate or deemed less advantageous. The safety and
effectiveness of Fosphenytoin Sodium Injection in this use has not been
systematically evaluated for more than five days.
Fosphenytoin Sodium Injection can be used for the control of generalized
convulsive status epilepticus and the prevention and treatment of
seizures occurring during neurosurgery. It can also be substituted,
short-term, for oral phenytoin.
About Abraxis BioScience, Inc.
Abraxis BioScience, Inc. is an integrated global biopharmaceutical
company dedicated to meeting the needs of critically ill patients. The
company develops, manufactures and markets one of the broadest
portfolios of injectable products and leverages revolutionary technology
such as its nab� platform to discover
and deliver breakthrough therapeutics that transform the treatment of
cancer and other life-threatening diseases. The first FDA approved
product to use this nab platform, ABRAXANE�,
was launched in 2005 for the treatment of metastatic breast cancer.
Abraxis trades on the Nasdaq Global Market under the symbol ABBI. For
more information about the company and its products, please visit www.abraxisbio.com.
Cerebyx� is a
registered trademark of Pfizer Inc.