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Goodwill and Other Intangibles
12 Months Ended
Dec. 31, 2011
Goodwill and Other Intangibles [Abstract]  
Goodwill and Intangible Assets Disclosure [Text Block]

Note 7: Goodwill and Other Intangibles

 

Goodwill at December 31 was as follows:

 

2011

2010

Goodwill

$1,434.7

$1,423.9

 

Substantially all of our goodwill balance is attributable to the human pharmaceutical business segment. See Note 3 for a further discussion of goodwill resulting from recent business combinations. No impairments occurred with respect to the carrying value of goodwill for the years ended December 31, 2011, 2010, or 2009.

 

The components of other intangible assets at December 31 were as follows:

 

 

 

 

 

 

 

 

 

 

2011

2010

 

 

 

Description

Carrying Amount – Gross

 

Accumulated Amortization

Carrying Amount – Net

Carrying Amount – Gross

 

Accumulated Amortization

Carrying Amount –Net

 

 

Finite-lived intangible assets

 

 

 

 

 

 

  Marketed products

$4,624.9

$(1,481.2)

$3,143.7

$3,789.1

$(1,023.4)

$2,765.7

  Other

117.3

(42.5)

74.8

62.5

(31.3)

31.2

Total finite-lived intangible assets

4,742.2

(1,523.7)

3,218.5

3,851.6

(1,054.7)

2,796.9

 

 

 

 

 

 

 

Indefinite-lived intangible assets

 

 

 

 

 

 

  In-process research and
    development

 

474.9

 

0.0

 

474.9

 

598.0

 

0.0

 

598.0

 

 

 

 

 

 

 

Total other intangible assets

$5,217.1

$(1,523.7)

$3,693.4

$4,449.6

$(1,054.7)

$3,394.9

 

Marketed products consists of the amortized cost of the rights to assets acquired in business combinations and approved for marketing in a significant global jurisdiction (U.S., Europe, and Japan) and capitalized milestone payments. Other intangibles consist primarily of the amortized cost of licensed platform technologies that have alternative future uses in research and development, manufacturing technologies, and customer relationships from business combinations. IPR&D consists of the acquisition date fair value of intangible assets acquired in business combinations that have not yet achieved regulatory approval for marketing. See Note 3 for a further discussion of indefinite-lived intangible assets acquired in recent business combinations.

 

The remaining weighted-average amortization period for finite-lived intangible assets is approximately 9 years. Amortization expense for 2011, 2010, and 2009 was $469.0 million, $385.7 million, and $277.0 million, respectively. The estimated amortization expense for our current finite-lived intangible assets for each of the five succeeding years approximates $530 million in 2012, $460 million in 2013, $410 million in 2014, $380 million in 2015, and $330 million in 2016. Amortization expense is included in either cost of sales or marketing, selling, and administrative depending on the nature of the intangible asset being amortized.

 

During 2011, we recorded impairment charges of $151.5 million due primarily to the partial impairment of the IPR&D assets related to Amyvid and liprotamase. The impairment of Amyvid was due to a delay in product launch and lower sales projections during the early part of the product's expected life cycle. In April 2011, we received a complete response letter from the FDA for the NDA for liprotamase, which communicated the need for us to conduct an additional clinical trial prior to a re-submission, resulting in an impairment of liprotamase.

 

No impairments occurred with respect to the carrying value of other intangible assets for the years ended December 31, 2010 and 2009.