BUFFALO GROVE, Ill.--(BUSINESS WIRE)--April 24, 2006--Akorn, Inc. (AMEX:AKN - News) today announced that it has received a supplemental new drug application (NDA) approval for Inapsine ® injection. Akorn is the NDA holder of this drug product. Inapsine ® has been off the market since 2001 due to compliance issues associated with the Decatur manufacturing facility. Akorn recently was awarded the Premier Purchasing Partners, LP contract for Inapsine ®. Premier is one of the nation’s largest hospital group purchasing organizations. The award is effective July 1, 2006.
Arthur S. Przybyl, Akorn’s President and Chief Executive Officer stated, “We are pleased to announce this product approval. We expect to launch Inapsine ® in June 2006".
About Akorn, Inc.
Akorn, Inc. manufactures and markets sterile specialty pharmaceuticals. Akorn has manufacturing facilities located in Decatur, Illinois and Somerset, New Jersey and markets and distributes an extensive line of hospital and ophthalmic pharmaceuticals. Additional information is available at the Company’s website at www.akorn.com.
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Contact: Akorn, Inc. Arthur S. Przybyl, 847-279-6100
Source: Akorn, Inc.
