Commission Regulation (EC) No 75/2005 of 18 January 2005 amending Annexes I, II and III to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin as regards moxidectin, linear alkyl benzene sulphonic acids with alkyl chain lengths ranging from C9 to C13, containing less than 2,5 % of chains longer than C13 and Acetylisovaleryltylosin
Proposed act with possible EEA relevance
Act under scrutiny by EEA EFTA
Draft Joint Committee Decision (JCD) under consideration
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Legal status
EU legal act incorporated into the EEA Agreement, but no longer in force in the Agreement Area (EEA Agreement)
II Technical Regulations, Standards, Testing and Certification
II.XIII Medicinal Products
Joint committee decision (JCD)
099/2005 In force in the EEA
No Legal documents
Commission Regulation (EC) No 75/2005 of 18 January 2005 amending Annexes I, II and III to Council Regulation (EEC) No 2377/90 laying down a Community procedure for the establishment of maximum residue limits of veterinary medicinal products in foodstuffs of animal origin as regards moxidectin, linear alkyl benzene sulphonic acids with alkyl chain lengths ranging from C9 to C13, containing less than 2,5 % of chains longer than C13 and Acetylisovaleryltylosin
Reglugerð framkvæmdastjórnarinnar (EB) nr. 75/2005 frá 18. janúar 2005 um breytingu á I., II. og III. viðauka við reglugerð ráðsins (EBE) nr. 2377/90 þar sem mælt er fyrir um sameiginlega aðferð til að ákvarða hámarksmagn leifa dýralyfja í matvælum úr dýraríkinu að því er varðar moxídektín, línulegar alkýlbensensúlfonsýrur, þar sem lengd alkýlkeðjanna er á bilinu C9 til C13 og innan við 2,5% keðjanna eru lengri en C13, og asetýlísóvalerýltýlósín
Verordnung (EG) Nr. 75/2005 der Kommission vom 18. Januar 2005 zur Änderung der Anhänge I, II und III der Verordnung (EWG) Nr. 2377/90 des Rates zur Schaffung eines Gemeinschaftsverfahrens für die Festsetzung von Höchstmengen für Tierarzneimittelrückstände in Nahrungsmitteln tierischen Ursprungs in Bezug auf Moxidectin, „Lineare Alkylbenzolsulfonsäuren mit Alkylkettenlängen im Bereich von C9 bis C13, mit einem Gehalt an Ketten länger als C13 von weniger als 2,5 %“ und Acetylisovaleryltylosin
Kommisjonsforordning (EF) nr. 75/2005 av 18. januar 2005 om endring av vedlegg I, II og III til rådsforordning (EØF) nr. 2377/90 om en framgangsmåte i Fellesskapet for fastsettelse av maksimumsgrenser for restmengder av veterinærpreparater i næringsmidler av animalsk opprinnelse med hensyn til moksidektin, lineære alkylbenzensulfonsyrer med alkylkjedelengder mellom C9 og C13, som inneholder mindre enn 2,5 % med alkylkjeder som er lengre enn C13, og acetylisovaleryltylosin
History
09.07.2005
Adopted JCD confirmed entry into force date
09.07.2005
Compliance date in the EEA
08.07.2005
Adoption of Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement
23.05.2005
Draft Joint Commitee Decision (JCD) incorporating the act into the EEA Agreement sent to Commission
18.01.2005
Adoption date in the EU
20.03.2005
Compliance date in the EU
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