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APP Pharmaceuticals, Inc., a leading provider of hospital-based injectable pharmaceutical products, said that the U.S Food and Drug Administration has approved APP's manufacturing facility in Barceloneta, Puerto Rico for the manufacture of three product codes of Heparin Sodium Injection, USP. "Bringing this third manufacturing site on-line is an important part of our commitment to ensuring that an uninterrupted and safe supply of heparin of the highest quality is available for U.S. patients," said Tom Silberg, chief executive officer of APP Pharmaceuticals.

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