| 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 | ||||||||
| Download and more information: |
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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
