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AVANIR Pharmaceuticals (FRA:AV2B) Total Liabilities : €26.07 Mil (As of Sep. 2014)


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What is AVANIR Pharmaceuticals Total Liabilities?

AVANIR Pharmaceuticals's Total Liabilities for the quarter that ended in Sep. 2014 was €26.07 Mil.

AVANIR Pharmaceuticals's quarterly Total Liabilities declined from Mar. 2014 (€40.46 Mil) to Jun. 2014 (€38.07 Mil) and declined from Jun. 2014 (€38.07 Mil) to Sep. 2014 (€26.07 Mil).

AVANIR Pharmaceuticals's annual Total Liabilities increased from Sep. 2012 (€38.16 Mil) to Sep. 2013 (€43.09 Mil) but then declined from Sep. 2013 (€43.09 Mil) to Sep. 2014 (€26.07 Mil).


AVANIR Pharmaceuticals Total Liabilities Historical Data

The historical data trend for AVANIR Pharmaceuticals's Total 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.

* Premium members only.

AVANIR Pharmaceuticals Total Liabilities Chart

AVANIR Pharmaceuticals Annual Data
Trend Sep05 Sep06 Sep07 Sep08 Sep09 Sep10 Sep11 Sep12 Sep13 Sep14
Total Liabilities
Get a 7-Day Free Trial Premium Member Only Premium Member Only 10.79 13.31 38.16 43.09 26.07

AVANIR Pharmaceuticals Quarterly Data
Dec09 Mar10 Jun10 Sep10 Dec10 Mar11 Jun11 Sep11 Dec11 Mar12 Jun12 Sep12 Dec12 Mar13 Jun13 Sep13 Dec13 Mar14 Jun14 Sep14
Total Liabilities Get a 7-Day Free Trial Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only Premium Member Only 43.09 38.20 40.46 38.07 26.07

AVANIR Pharmaceuticals Total Liabilities Calculation

Total Liabilities are the liabilities that the company has to pay others. It is a part of the balance sheet of a company that shareholders do not own, and would be obligated to pay back if the company liquidated.

AVANIR Pharmaceuticals's Total Liabilities for the fiscal year that ended in Sep. 2014 is calculated as

Total Liabilities=Total Current Liabilities+Total Noncurrent Liabilities
=Total Current Liabilities+(Long-Term Debt & Capital Lease Obligation+Other Long-Term Liabilities
=24.904+(0+1.165
+NonCurrent Deferred Liabilities+PensionAndRetirementBenefit)
+0+0)
=26.07

Total Liabilities=Total Assets (A: Sep. 2014 )-Total Equity (A: Sep. 2014 )
=238.219-212.15
=26.07

AVANIR Pharmaceuticals's Total Liabilities for the quarter that ended in Sep. 2014 is calculated as

Total Liabilities=Total Current Liabilities+Total Noncurrent Liabilities
=Total Current Liabilities+(Long-Term Debt & Capital Lease Obligation+Other Long-Term Liabilities
=24.904+(0+1.165
+NonCurrent Deferred Liabilities+PensionAndRetirementBenefit)
+0+0)
=26.07

Total Liabilities=Total Assets (Q: Sep. 2014 )-Total Equity (Q: Sep. 2014 )
=238.219-212.15
=26.07

* 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.


AVANIR Pharmaceuticals Total Liabilities Related Terms

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AVANIR Pharmaceuticals (FRA:AV2B) Business Description

Traded in Other Exchanges
N/A
Address
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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