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Identifiable Intangible Assets
6 Months Ended
Jun. 30, 2022
Identifiable Intangible Assets
NOTE 5 – Identifiable intangible assets:
Identifiable intangible assets consisted of the following:
 
 
  
Gross carrying amount net

of impairment
 
  
Accumulated

amortization
 
  
Net carrying amount
 
 
  
June 30,
 
  
December 31,
 
  
June 30,
 
  
December 31,
 
  
June 30,
 
  
December 31,
 
 
  
2022
 
  
2021
 
  
2022
 
  
2021
 
  
2022
 
  
2021
 
 
  
(U.S. $ in millions)
 
Product rights
   $ 17,987      $ 18,815      $ 12,181      $ 12,318      $ 5,806      $ 6,497  
Trade names
     570        590        211        198        359        392  
In process research and development
     535        577        —          —          535        577  
    
 
 
    
 
 
    
 
 
    
 
 
    
 
 
    
 
 
 
Total
   $ 19,092      $ 19,982      $ 12,392      $ 12,516      $ 6,700      $ 7,466  
    
 
 
    
 
 
    
 
 
    
 
 
    
 
 
    
 
 
 
Product rights and trade names
Product rights and trade names are assets presented at amortized cost. Product rights and trade names represent a portfolio of pharmaceutical products from various therapeutic categories from various acquisitions with a weighted average life of approximately 10 years.
Amortization of intangible assets was $212 million and $173 million in the three months ended June 30, 2022 and 2021, respectively.
Amortization of intangible assets was $412 million and $414 million in the six months ended June 30, 2022 and 2021, respectively.
IPR&D
Teva’s IPR&D are assets that have not yet been approved in major markets. Teva’s IPR&D is comprised mainly of various generic products from the Actavis Generics acquisition of $503 million. IPR&D carries intrinsic risks that the asset might not succeed in advanced phases and may be impaired in future periods.
Intangible assets impairments
Impairments of long-lived intangible assets for the three months ended June 30, 2022 and 2021 were $51 million and $195 million, respectively.
Impairments in the second quarter of 2022 consisted of:
 
  (a)
Identifiable product rights of $32 million related to updated market assumptions regarding price and volume of products acquired from Actavis Generics, and
 
  (b)
IPR&D assets of $19 million due to generic pipeline products acquired from Actavis Generics resulting from development progress and changes in other key valuation indications (e.g., market size, competition assumptions, legal landscape, launch date).
Impairments in the second quarter of 2021 consisted of:
 
  (a)
Identifiable product rights of $168 million due to:
(i) $138 million, mainly related to updated market assumptions regarding price and

volume of products acquired from Actavis Generics that are primarily marketed in the United States, and (ii)
$30 million related to

lenalidomide (generic equivalent of Revlimid
®
), resulting from modified competition assumptions as a result of settlements between the

innovator and other generic filers, and 
 
  (b)
IPR&D assets of $27 million due to generic pipeline products acquired from Actavis Generics resulting from development progress and changes in other key valuation indications (e.g., market size, competition assumptions, legal landscape, launch date) in the United States.
Impairments of long-lived intangible assets for the six months ended June 30, 2022 and 2021 were $199 million and $274 million, respectively.
 
Impairments in the first
six
months of
2022
consisted mainly of:
 
  (a)
Identifiable product rights of $161 million related to updated market assumptions regarding price and volume of products acquired from Actavis Generics, and
 
  (b)
IPR&D assets of $21 million due to generic pipeline products acquired from Actavis Generics resulting from development progress and changes in other key valuation indications (e.g., market size, competition assumptions, legal landscape, launch date) in the United States.
Impairments in the first six months of 2021 consisted of:
 
  (a)
Identifiable product rights of $196 million
due to: (i) $166 million
, mainly related to updated market assumptions regarding price and

volume of products acquired from Actavis Generics that are primarily marketed in the United States
,
 and (ii)
$30 million related to lenalidomide (generic equivalent of Revlimid
®
), resulting from modified competition assumptions as a result of settlements between the innovator and other generic filers
.
 
  (b)
IPR&D assets of $78 million, due to generic pipeline products acquired from Actavis Generics resulting from development progress and changes in other key valuation indications (e.g., market size, competition assumptions, legal landscape, launch date) in the United States.
The fair value measurement of the impaired intangible assets in the first six months of 2022 is based on significant unobservable inputs in the market and thus represents a Level 3 measurement within the fair value hierarchy. The discount rate applied ranged from 7.25% to 8.25%. A probability of success factor ranging from 20% to 90% was used in the fair value calculation to reflect inherent regulatory and commercial risk of IPR&D.