National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 9) 2025

Administered by Department of Health, Disability and Ageing

Legislation au F2025L01217 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

 

National Health Act 1953

 

National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 9) 2025

 

PB 115 of 2025

 

Authority

 

This instrument, made under subsection 85AB(1) of the National Health Act 1953 (the Act), amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021)  (the Principal Determination).

 

The Principal Determination provides for the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS).

 

Purpose

 

This instrument makes amendments to the Principal Determination.

 

The Act provides that PBS listed drugs may be assigned to formularies identified as F1 and F2. F1 is intended for single branded drugs and F2 for drugs that have multiple brands, or are in a therapeutic group with other drugs with multiple brands. Drugs on F2 are subject to the provisions of the Act relating to price disclosure and guarantee of supply.

 

Section 84AC of the Act provides that a drug is on F1 or F2 if there is a determination in force under section 85AB that the drug is on F1 or F2.

 

Subsection 85AB(1) of the Act empowers the Minister (or delegate) to determine by legislative instrument that a listed drug is on F1 or F2. For a drug to be on F1, it must satisfy the criteria in subsection 85AB(4). This requires that there are no listed brands of pharmaceutical items that have the drug that are bioequivalent or biosimilar, and no listed brands of pharmaceutical items that have another drug in the same therapeutic group as the first drug that are bioequivalent or biosimilar. It also requires that the drug was not on F2 the day before the determination comes into effect. A drug may only be determined to be on F2 if it does not satisfy one or more of the criteria for F1 (subsection 85AB(3)).

 

When subsection 85AB(5) of the Act applies, which relates to listed drugs with a single brand combination item on the PBS, the listed drug is not placed on F1 or F2, but on the administrative combination drug list (CDL).

 

This instrument amends the Principal Determination by adding to F1 two new drugs, capivasertib and lumasiran from 1 October 2025. In addition, two drugs, adefovir and ketoprofen are being removed from F2 as these drugs will no longer be PBS listed from
1 October 2025.

 

 

 

 

Variation and revocation

 

Unless there is an express power to revoke or vary PB 33 of 2021 cited in this instrument, subsection 33(3) of the Acts Interpretation Act 1901 is relied upon to revoke or vary PB 33 of 2021.

 

Consultation

 

This instrument affects pharmaceutical companies with new medicines listing on the PBS.  Two new drugs, capivasertib and lumasiran meet the criteria for F1 under subsection 85AB(4). The drugs, adefovir and ketoprofen are being removed from F2 as these drugs will no longer be listed on the PBS, the PBAC advised that the delisting of these medicines would not result in unmet clinical need.

 

Before a drug is PBS listed and allocated to a formulary, there are detailed consultations about the drug with the responsible person and recommendations from the Pharmaceutical Benefits Advisory Committee (PBAC). Any PBAC recommendation is made following receipt of a submission made by the affected pharmaceutical company. Two-thirds of the PBAC membership is from the following interests or professions: consumers, health economists, practising community pharmacists, general practitioners, clinical pharmacologists and medical specialists.

 

No additional consultation with experts was undertaken regarding this determination because consultation with the affected responsible persons and the PBAC drew on the knowledge of persons with relevant expertise.

 

Commencement

 

This instrument commences on 1 October 2025.

 

This instrument is a legislative instrument for the purposes of the Legislation Act 2003.

 

Statement of Compatibility with Human Rights

Prepared in accordance with Part 3 of the Human Rights (Parliamentary Scrutiny) Act 2011

National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 9) 2025
(PB 115 of 2025)

This legislative instrument is compatible with the human rights and freedoms recognised or declared in the international instruments listed in section 3 of the Human Rights (Parliamentary Scrutiny) Act 2011.

Overview of the Legislative Instrument

This legislative instrument is made pursuant to subsection 85AB(1) of the National Health Act 1953 (the Act), which relates to listed drugs on F1 or F2. This instrument amends the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021) (the Principal Determination) which provides for the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS).

 

This instrument amends the Principal Determination by adding to F1 two new drugs, capivasertib and lumasiran from 1 October 2025. In addition, two drugs, adefovir and ketoprofen are being removed from F2 as these drugs will no longer be PBS listed from
1 October 2025.

 

Human rights implications

 

This legislative instrument engages Articles 2 and 12 of the International Covenant on Economic, Social and Cultural Rights by assisting with the progressive realisation by all appropriate means of the right of everyone to the enjoyment of the highest attainable standard of physical and mental health.

 

The PBS assists with the advancement of this human right by providing for subsidised access of medicines to patients. The recommendatory role of the PBAC ensures that decisions about subsidised access to medicines on the PBS are evidence-based.

 

The right to social security is contained in Article 9 of the International Covenant on Economic Social and Cultural Rights (ICESCR). It requires that a country must, within its maximum available resources, ensure access to a social security scheme that provides a minimum essential level of benefits to all individuals and families that will enable them to acquire at least essential health care. Countries are obliged to demonstrate that every effort has been made to use all resources that are at their disposal in an effort to satisfy, as a matter of priority, this minimum obligation.

 

The UN Committee on Economic Social and Cultural Rights reports that there is a strong presumption that retrogressive measures taken in relation to the right to social security are prohibited under ICESCR. In this context, a retrogressive measure would be one taken without adequate justification that had the effect of reducing existing levels of social security benefits, or of denying benefits to persons or groups previously entitled to them. However, it is legitimate for a government to re-direct its limited resources in ways that it considers to be more effective at meeting the general health needs of all society, particularly the needs of the more disadvantaged members of society.

 

Conclusion

 

This legislative instrument is compatible with human rights. Human rights continue to be protected by retaining clinically important medicines on the PBS and placing them in formularies that ensure the most cost-effective pricing for supply of each medicine to Australians.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 Rebecca Richardson

 Assistant Secretary

PBS Listing, Pricing and Policy Branch

Technology Assessment and Access Division

Department of Health, Disability and Ageing

Overview

The National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 9) 2025 was enacted to amend the National Health (Listed Drugs on F1 or F2) Determination 2021. This amendment, introduced under subsection 85AB(1) of the National Health Act 1953, pertains to the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS). The objective of this determination is to ensure that PBS listed drugs are appropriately assigned to formularies based on criteria such as brand exclusivity and therapeutic grouping. Two new drugs, capivasertib and lumasiran, are added to F1 starting from 1 October 2025, while adefovir and ketoprofen are removed from F2 as they will cease to be listed on the PBS. This amendment ensures that the PBS continues to provide cost-effective access to essential medicines while maintaining a balanced approach to drug formulary management.

Scope and Application

The National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 9) 2025 amends the National Health (Listed Drugs on F1 or F2) Determination 2021, which governs the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS). This instrument, made under the authority of the National Health Act 1953, specifically alters the Principal Determination by adding two new drugs, capivasertib and lumasiran, to F1 from 1 October 2025, and by removing two drugs, adefovir and ketoprofen, from F2 as they will no longer be listed on the PBS from the same date. The changes apply to pharmaceutical companies and entities involved in the PBS, ensuring that the drugs are priced and supplied in the most cost-effective manner to Australians. The instrument also ensures compliance with human rights obligations by maintaining access to essential medicines while adjusting the formularies to enhance cost-effectiveness and ensure the highest attainable standard of health.

Key Provisions

The main operative sections of the National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 9) 2025 involve amendments to the National Health (Listed Drugs on F1 or F2) Determination 2021 (subsection 85AB(1) of the National Health Act 1953). These amendments are designed to update the allocation of drugs within the Pharmaceutical Benefits Scheme (PBS) formularies. Specifically, the instrument adds two new drugs, capivasertib and lumasiran, to the F1 formulary, which is intended for single branded drugs (section 85AB(4)). Conversely, two drugs, adefovir and ketoprofen, are being removed from the F2 formulary, which is designated for drugs with multiple brands or those within therapeutic groups containing multiple brands, as they will no longer be listed on the PBS from 1 October 2025. The obligations and requirements imposed by the Act on the parties it governs include ensuring that drugs are appropriately allocated to the F1 or F2 formularies based on specific criteria. For a drug to be placed on the F1 formulary, it must meet stringent criteria that there are no bioequivalent or biosimilar listed brands of the drug or any drug in the same therapeutic group, and it must not have been on F2 the day before the determination comes into effect. For F2, the drug must not satisfy the criteria for F1. The Pharmaceutical Benefits Advisory Committee (PBAC) plays a crucial role in this process, providing recommendations on drug listings and ensuring that decisions are evidence-based. Pharmaceutical companies must also comply with the requirements of the Act by providing necessary information and engaging in consultations with the relevant authorities. Any breaches of the provisions in this instrument can lead to civil or criminal consequences. While the specific penalties are not outlined in the Explanatory Statement, breaches of similar legislative instruments under the National Health Act 1953 can result in significant fines and potential imprisonment. For instance, under section 16 of the Act, penalties can include fines of up to $22,200 for individuals and up to $111,000 for corporations, along with imprisonment terms for more serious offences. The instrument also ensures that any amendments are made in compliance with human rights obligations, particularly those related to the right to health and social security, as outlined in international covenants and conventions.

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Sourced from the Federal Register of Legislation at 26 August 2026. For the latest information on Australian Government law please go to https://www.legislation.gov.au.