THERAPEUTIC GOODS ACT 1989
SECTION 14 AND 14A NOTICE
On January 24 2013 the delegate of the Secretary of the Department of Health and Ageing for the purposes of subsection 14 and 14A of the Therapeutic Goods Act 1989 (“the Act”) gave his consent to:
(a) the supply of the product Sustanon 250 Injection ampoule [Aust R 14521], by Merck Sharp & Dohme Australia Pty Ltd North Ryde NSW (“the Company”);
That does not conform with paragraph 3(2)(1) of Therapeutic Goods Order (TGO) 69, in that the details of the previous sponsor (Schering-Plough) are used on the ampoule and carton labels, instead of the details of the Company.
Pursuant to subsection 15(1) of the Act, the consent given by the delegate of the Secretary as described above is subject to the following conditions:
- The consent to supply applies to batches 163218 and 247049 of the product.
2. The labels to which this consent applies are identical to those currently used, having the previous sponsor details.
3. No other changes have been made to the product Sustanon 250 Injection ampoule [Aust R 14521].
4. Arrangements are in place to ensure complaints or queries concerning this product will be dealt with promptly.