(1) For paragraph 136F(1)(d) of the Act, the following shipment information is prescribed in relation to each shipment of a pharmaceutical product:
(a) the name of the pharmaceutical product;
(b) the amount of the product in the shipment;
(c) the name of the licensee;
(d) the licensee's address for service;
(e) the name of the eligible importing country;
(f) if a person is importing the pharmaceutical product on behalf of, and with the authorisation of, the eligible importing country--the name and address of the person;
(g) a description of the packaging (including colour, size and shape) and the labelling or marking of the pharmaceutical product.
(2) For paragraph 136F(1)(d) of the Act, the shipment information must be made available for at least the duration of the licence.