ANNEXU.K.

In Table 1 of the Annex to Regulation (EU) No 37/2010, an entry for the following substance is inserted in alphabetical order:

Pharmacologically active SubstanceMarker residueAnimal SpeciesMRLTarget TissuesOther Provisions (according to Article 14(7) of Regulation (EC) No 470/2009)Therapeutic Classification
‘Porcine prolactinNOT APPLICABLEPorcineNo MRL requiredNOT APPLICABLE

For oral use in newborn piglets at a dose of up to 0,2 mg/animal.

For use in sows at a total dose of up to 5 mg/animal.

Agents acting on the reproductive system’