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| European Public Assessment Report | Revision 1 - Published 14/10/09 |
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| BG | ES | CS | DA | DE | ET | EL | EN | FR | IT | LV | LT | HU | MT | NL | PL | PT | RO | SK | SL | FI | SV | See Glossary of language codes... | |||
| u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | Summary for the public | |||
| u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | All Authorised Presentations | |||
| u | Public assessment report (6) | ||||||||||||||||||||||||
| u | Procedural steps taken and scientific information after authorisation (8) | ||||||||||||||||||||||||
| Product Information* | |||||||||||||||||||||||||
| 30/09/2009 Clopidogrel Teva-H-C-1053-IA-01 | |||||||||||||||||||||||||
| BG | ES | CS | DA | DE | ET | EL | EN | FR | IT | LV | LT | HU | MT | NL | PL | PT | RO | SK | SL | FI | SV | See Glossary of language codes... | |||
| u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | u | ||||
(*)This document includes: Please note that the size of the above document can
exceed 50 pages. |
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EPARs for authorised medicinal products for human use |