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Therapeutic Goods (Standard for MDMA) (TGO 112) Order 2024
In force
Administered by
Department of Health, Disability and Ageing
This item is authorised by the following title:
Therapeutic Goods Act 1989
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F2024L01036
20 August 2024
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Part 1Preliminary
1 Name
2 Commencement
3 Authority
4 Definitions
USP means the United States Pharmacopeia-National Formulary. 5 Standard
6 Application
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Part 2Requirements for MDMA hydrochloride
7 Application of this Part
8 Assay limits
9 Tests
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Part 3Requirements for MDMA hydrochloride products
10 Application of this Part
11 General
12 Assay limits
13 Tests
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14 Information to be included on the label
Schedule 1—Specified tests for MDMA hydrochloride
Schedule 2—Specified tests for MDMA hydrochloride products
