COMMONWEALTH OF AUSTRALIA
Department of Health
Therapeutic Goods Administration
THERAPEUTIC GOODS ACT 1989
Section 14 and 14A Notice
On 29 June 2015, the delegate of the Secretary of the Department of Health for the purposes of subsection 14 and 14A of the Therapeutic Goods Act 1989 (“the Act”), on the application of Biogen Australia Pty Ltd, gave consent to the importation and supply of
- fampridine (FAMPYRA) modified release tablet 10 mg in bottle [AUST R 170002],
Batches 75888, 75889, 76162, 76476, 76477, 77505 & 77519
that does not conform with the requirements of paragraph 3(2)(l) of the Therapeutic Goods Order No. 69- General requirements for labels for medicines, in that the sponsor name on the label is not that currently registered (no change in address details).
The consent is effective from 29 June 2015 until the exhaustion of supply of the above-nominated batches of the product.
The delegate of the Secretary, under subsection 15(1) of the Act, made the consent subject to the following conditions:
- The labels to which this consent applies are those currently approved for the product.