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<ep-patent-document id="EP20200633B8W1" file="EP20200633W1B8.xml" lang="en" country="EP" doc-number="3825306" kind="B8" correction-code="W1" date-publ="20230802" status="c" dtd-version="ep-patent-document-v1-6">
<SDOBI lang="en"><B000><eptags><B001EP>ATBECHDEDKESFRGBGRITLILUNLSEMCPTIESILTLVFIRO..CY..TRBGCZEEHUPLSK..HRIS..MTNO........................</B001EP><B005EP>J</B005EP><B007EP>2.0.21 -  2999001/0</B007EP></eptags></B000><B100><B110>3825306</B110><B120><B121>CORRECTED EUROPEAN PATENT SPECIFICATION</B121></B120><B130>B8</B130><B132EP>B1</B132EP><B140><date>20230802</date></B140><B150><B151>W1</B151><B153>73</B153><B155><B1551>de</B1551><B1552>Bibliographie</B1552><B1551>en</B1551><B1552>Bibliography</B1552><B1551>fr</B1551><B1552>Bibliographie</B1552></B155></B150><B190>EP</B190></B100><B200><B210>20200633.4</B210><B220><date>20080430</date></B220><B240><B241><date>20201007</date></B241></B240><B250>en</B250><B251EP>en</B251EP><B260>en</B260></B200><B300><B310>91513007 P</B310><B320><date>20070501</date></B320><B330><ctry>US</ctry></B330><B310>91666207 P</B310><B320><date>20070508</date></B320><B330><ctry>US</ctry></B330><B310>97604407 P</B310><B320><date>20070928</date></B320><B330><ctry>US</ctry></B330></B300><B400><B405><date>20230802</date><bnum>202331</bnum></B405><B430><date>20210526</date><bnum>202121</bnum></B430><B450><date>20230607</date><bnum>202323</bnum></B450><B452EP><date>20221104</date></B452EP><B480><date>20230802</date><bnum>202331</bnum></B480></B400><B500><B510EP><classification-ipcr sequence="1"><text>C07D 221/28        20060101AFI20220331BHEP        </text></classification-ipcr><classification-ipcr sequence="2"><text>C07B  59/00        20060101ALI20220331BHEP        </text></classification-ipcr><classification-ipcr sequence="3"><text>A61K  31/439       20060101ALI20220331BHEP        </text></classification-ipcr><classification-ipcr sequence="4"><text>A61P  11/14        20060101ALI20220331BHEP        </text></classification-ipcr></B510EP><B520EP><classifications-cpc><classification-cpc sequence="1"><text>C07B  59/002       20130101 LI20130101BHEP        </text></classification-cpc><classification-cpc sequence="2"><text>C07D 471/08        20130101 LI20130101BHEP        </text></classification-cpc><classification-cpc sequence="3"><text>A61K  31/195       20130101 FI20150707BHEP        </text></classification-cpc><classification-cpc sequence="4"><text>A61K  31/4709      20130101 LI20131114BHEP        </text></classification-cpc><classification-cpc sequence="5"><text>A61K  31/485       20130101 LI20140424BHEP        </text></classification-cpc><classification-cpc sequence="6"><text>A61K  31/49        20130101 LI20141106BHEP        </text></classification-cpc><classification-cpc sequence="7"><text>C07D 221/28        20130101 LI20150707BHEP        </text></classification-cpc><classification-cpc sequence="8"><text>G01N  33/491       20130101 LI20170209BHEP        </text></classification-cpc><classification-cpc sequence="9"><text>G01N  33/493       20130101 LI20170209BHEP        </text></classification-cpc><classification-cpc sequence="10"><text>A61P  11/00        20180101 LI20200318BHEP        </text></classification-cpc><classification-cpc sequence="11"><text>A61P  11/14        20180101 LI20200319BHEP        </text></classification-cpc><classification-cpc sequence="12"><text>A61P  25/00        20180101 LI20200323BHEP        </text></classification-cpc></classifications-cpc></B520EP><B540><B541>de</B541><B542>MORPHINANVERBINDUNGEN</B542><B541>en</B541><B542>MORPHINAN COMPOUNDS</B542><B541>fr</B541><B542>COMPOSÉS DE MORPHINANE</B542></B540><B560><B562><text>G. HEINKELE ET. AL.: "Synthesis of [2H3]-dextromethorphan and its major urinary metabolites [2H3]-dextrorphan and [2H3]-dextrorphan-beta-glucoronide", JOURNAL OF LABELLED COMPOUNDS AND RADIOPHARMACEUTICALS, vol. 45, 2002, pages 1153-1158, XP002490642, DOI: 10.1002/jlcr.640</text></B562><B562><text>T.H. EICHHOLD ET. AL.: "Highly sensitive high-peformance liquid chromatographic-tandem mass spectrometric method for the analysis of dextromorphan in human plasma.", JOURNAL OF CHROMATOGRAPHY B, vol. 698, 1997, pages 147-154, XP002490644,</text></B562><B562><text>G. HEINKELE ET. AL.: "Synthesis of [2H]-labelled phase I metabolites using 1-[2H]-pyridinium hydrochloride.", JOURNAL OF LABELLED COMPOUNDS AND RADIOPHARMACEUTICALS, vol. 48, 2005, pages 457-461, XP002490645, DOI: 10.1002/jlcr.941</text></B562><B562><text>H. BÖLCSKEI ET. 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