Therapeutic Goods Act 1989
Therapeutic Goods (Listing) Notice 2012 (No. 1)
I, BRIAN RICHARDS, National Manager (Acting) of the Therapeutic Goods Administration, delegate of the Minister for Health for the purposes of subsection 9A(5) of the Therapeutic Goods Act 1989 (the Act) and acting under that provision, require the following therapeutic goods to be included in the part of the Australian Register of Therapeutic Goods (the Register) for listed goods:
· preparations, for the purpose of Item 3, Part 1 of Schedule 4 to the Therapeutic Goods Regulations 1990 (the Regulations), that contain ‘sodium molybdate dihydrate’ as a therapeutically active ingredient, subject to the following conditions:
o the preparations are for oral use only; and
o the preparations provide not more than 125 μg of molybdenum per daily dose.
This Notice commences from the day after it is registered on the Federal Register of Legislative Instruments.
Pursuant to subsection 9A(6) of the Act, this Notice ceases to have effect on the day that amendments to the Regulations come into effect to require inclusion of the therapeutic goods listed in this Notice in the part of the Register for listed goods.
Dated this 1st day of May 2012
Delegate of the Minister for Health