8AKInformation to be given in notice to holder

8AK Information to be given in notice to holder

For paragraph 8F(2)(e) of the Code, the following information is prescribed for a notice given to a holder under subsection 8F(1) of the Code: (a) for the approval of an active constituent: (i) the information required by section 8H of the Code in relation to the approval; and (ii) the date of the approval under section 22 of the Code; and (iii) the date on which the notice is given to the holder; and (iv) any other details entered in the Record about the active constituent that the APVMA thinks appropriate; (b) for the registration of a chemical product: (i) the information required by section 8H of the Code in relation to the registration; and (ii) the date of the registration under section 22 of the Code; and (iii) the distinguishing name of the chemical product; and (iv) the date on which the notice is given to the holder; and (v) any other details about the chemical product, entered in the Register, that the APVMA thinks appropriate; (c) for the approval of a label: (i) the date of the approval under section 22 of the Code; and (ii) the distinguishing number of the label; and (iii) the date on which the notice is given to the holder; and (iv) any other details about the label, entered in the relevant APVMA file, that the APVMA thinks appropriate; (d) for the variation of a relevant particular or condition: (i) the information required by section 8J of the Code in relation to the variation; and (ii) the date of the variation under section 22 of the Code; and (iii) the date on which the notice is given to the holder; and (iv) for a variation of a relevant particular or condition of an approval of an active constituent—any other details entered in the Record about the active constituent that the APVMA thinks appropriate; and (v) for a variation of a relevant particular or condition of a registration of a chemical product—any other details about the chemical product, entered in the Register, that the APVMA thinks appropriate; and (vi) for a variation of a relevant particular or condition of an approval of a label—any other details about the label, entered in the relevant APVMA file, that the APVMA thinks appropriate.