European Case Law Identifier: | ECLI:EP:BA:2010:R001609.20100519 | ||||||||
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Date of decision: | 19 May 2010 | ||||||||
Case number: | R 0016/09 | ||||||||
Petition for review of: | T 0764/06 | ||||||||
Application number: | 96924368.2 | ||||||||
IPC class: | C07D 207/34 | ||||||||
Language of proceedings: | EN | ||||||||
Distribution: | B | ||||||||
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Title of application: | Crystalline R-(R*,R*)-2-(4-fluorophenyl)-beta, delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-(phenylamino) carbonyl-1H-pyrrole-1-heptanoic acid hemi calcium salt (atorvastatin) | ||||||||
Applicant name: | Warner-Lambert Company LLC | ||||||||
Opponent name: | Teva Pharmaceutical Industries Ltd. LEK Pharmaceutical and Chemical Company d.d. |
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Board: | EBA | ||||||||
Headnote: | - | ||||||||
Relevant legal provisions: |
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Keywords: | Petition for review - clearly unallowable | ||||||||
Catchwords: |
See paragraph 2.2.13 |
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Source: http://www.epo.org/law-practice/case-law-appeals/recent/r090016eu1.html
Date retrieved: 17 May 2021