AVANIR Pharmaceuticals (FRA:AV2B) Other Long-Term Liabilities : €1.16 Mil (As of Sep. 2014)

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What is AVANIR Pharmaceuticals Other Long-Term Liabilities?

AVANIR Pharmaceuticals's other long-term liabilities for the quarter that ended in Sep. 2014 was €1.16 Mil.

AVANIR Pharmaceuticals's quarterly other long-term liabilities increased from Mar. 2014 (€1.46 Mil) to Jun. 2014 (€1.59 Mil) but then declined from Jun. 2014 (€1.59 Mil) to Sep. 2014 (€1.16 Mil).

AVANIR Pharmaceuticals's annual other long-term liabilities increased from Sep. 2012 (€0.52 Mil) to Sep. 2013 (€1.04 Mil) and increased from Sep. 2013 (€1.04 Mil) to Sep. 2014 (€1.16 Mil).

AVANIR Pharmaceuticals Other Long-Term Liabilities Historical Data

The historical data trend for AVANIR Pharmaceuticals's Other Long-Term Liabilities can be seen below:

* For Operating Data section: All numbers are indicated by the unit behind each term and all currency related amount are in USD.
* For other sections: All numbers are in millions except for per share data, ratio, and percentage. All currency related amount are indicated in the company's associated stock exchange currency.

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AVANIR Pharmaceuticals Other Long-Term Liabilities Chart

AVANIR Pharmaceuticals Annual Data

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Other Long-Term Liabilities

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AVANIR Pharmaceuticals Quarterly Data
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AVANIR Pharmaceuticals Other Long-Term Liabilities Calculation

Other Long-Term Liabilities are the other liabilities on the balance sheet that do not need to be repaid within the next 12 months, but still need to be repaid over time. For instance, on Wal-Mart's balance sheet, there are items called Long Term obligations under capital leases, deferred income taxes, and redeemable non-controlling interest. These are all Other Long-Term Liabilities.

AVANIR Pharmaceuticals Other Long-Term Liabilities Related Terms

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AVANIR Pharmaceuticals (FRA:AV2B) Business Description

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http://www.avanir.com

Avanir Pharmaceuticals was incorporated in California in August 1988 and was reincorporated in Delaware in March 2009. The Company is a biopharmaceutical company focused on acquiring, developing and commercializing novel therapeutic products for the treatment of central nervous system disorders. The Company commenced promotion of NUEDEXTA in the United States in February 2011. The Company is also studying AVP-923 for use in different types of neuropathic pain. NUEDEXTA is the first and only FDA-approved treatment for pseudobulbar affect. NUEDEXTA is an combination of two components: dextromethorphan hydrobromide, the ingredient that is harmacologically active in the central nervous system, and quinidine sulfate, a metabolic inhibitor enabling dextromethorphan to reach therapeutic plasma concentrations. The Company currently markets NUEDEXTA to approximately 10,000 physicians and other healthcare providers who specialize in psychiatry, neurology or geriatric medicine and practice in outpatient or long-term care settings. NUEDEXTA may face competition from several products: Antidepressants, including Prozac, Celexa, Zoloft, Paxil, Elavil and Pamelor and others; Atypical antipsychotic agents, including Zyprexa, Risperdal, Seroquel, Abilify, Geodon and others; and Miscellaneous agents, including Symmetrel, Lithium and others. The Company is subject to regulation under the Occupational Safety and Health Act, the Environmental Protection Act, the Toxic Substance Control Act, the Export Control Act and other present and future laws of general application.

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