How to apply for a permit to export narcotic, psychotropic and precursor substances

Check one box to indicate whether the controlled substance you are proposing to export is a raw material (for example a bulk substance for further manufacturing) or a finished good (for example a pharmaceutical preparation).

Licence holder’s name

Permits to export controlled substances can only be issued to exporters who hold a licence to export substances covered by Regulation 10 and 10A of the Customs (Prohibited Exports) Regulations 1958. State the name of the licence holder.

Company name

State your company’s name

Export licence number

State your export licence number which can be found on your licence issued by NCS.

Approximate date of export

Indicate the expected export date for the consignment if the export permit is issued. If the exact date is not known, provide the approximate time period (e.g. Oct 2022).

Company address

State the physical address to be displayed on the export permit

Postal address

State the postal address to which you would like the export permit sent. Permits will be sent by standard mail unless an express post envelope accompanies the application.

Overseas importer’s full name

State the full name of the overseas importer

Overseas importer’s address

State the physical address of the overseas importer to be displayed on the export permit

Import authorisation No.

Narcotic and psychotropic substances that are subject to control under the international drug treaties cannot be exported from a country without the prior approval of the competent authority in the receiving country.

State the import authorisation number listed on the authorisation issued by the competent authority in the destination country. A scanned copy of the overseas import authorisation must accompany the export permit application submitted to NCS.

Import authorisation date of issue

Specify the date the overseas import permit was issued.

Substance name

Provide the name of the drug (e.g. morphine sulphate)

Trade name

If a finished good, provide the trade name of the goods.

Concentration/Strength

Indicate the concentration/strength of the controlled substance, e.g.

• Raw material: for assayable substances include the assay amount i.e. 98%
• Finished goods: show the amount of controlled substance in the preparation, for example mg/mL for liquids or mg per tablet for tablet products. The concentration should be in metric units.

Form of substance

Indicate the form of the finished goods, for example tablets, capsules, vials, ampoules etc.

Pack type and size

Provide details on the pack type and the size

• Raw material: for example, 25 kg drum
• Finished goods: for example; 24 tablet blister pack; 100 mL bottle; box of 100 tablets; box of 6 x 2mL ampoules.

Total number of packs in shipment

Specify the total number of packs (as defined above) that make up the proposed shipment. For example 25 packs of 24 tablets; 100 bottles of 100 mL; 1000 boxes of 100 tablets, 250 boxes of ampoules.

ARTG / APVMA / Laboratory Use

The ARTG No. (Australian Register of Therapeutic Goods) refers to the number allocated to all TGA-approved therapeutic goods (including export-only listings). The ARTG number must be provided for all exported finished goods that have a therapeutic claim. This is not applicable to raw materials.

The APVMA Product No. (Australian Pesticides and Veterinary Medicines Authority) applies to all approved pesticides and veterinary products. If the APVMA number is not available a copy of the APVMA permission or permit must be provided. This is not applicable to raw materials.

Laboratory Use – Material that will be used for laboratory or research purposes only.

Make sure you read and understand the declaration and consent. Sign the application form. Complete the contact details of the person signing the form. The form must be signed by the licence holder or a person that the licence holder has authorised in writing to make applications under the licence.