National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 6) 2025

Administered by Department of Health, Disability and Ageing

Legislation au F2025L00779 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. 6) 2025

 

PB 79 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, ivosidenib and maribavir from 1 July 2025. In addition, one drug, hypromellose with carbomer 980 is being removed from F2 as this drug will no longer be PBS listed from1 July 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, ivosidenib and maribavir meet the criteria for F1 under subsection 85AB(4).

The drug, hypromellose with carbomer 980 is being removed from F2 as this drug will no longer be listed on the PBS, the PBAC advised the delisting of this medicine would not result in an 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 July 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. 6) 2025
(PB 79 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, ivosidenib and maribavir from 1 July 2025. In addition, one drug, hypromellose with carbomer 980 is being removed from F2 as this drug will no longer be PBS listed from
1 July 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

Pricing and PBS 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. 6) 2025 is a legislative instrument enacted to amend 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 amendment was introduced by the Australian Parliament to address the need for timely updates to the PBS list of medications, ensuring that the scheme remains effective and responsive to changes in medical needs and market availability. The National Health Act 1953 empowers the Minister for Health to make such determinations through legislative instruments, facilitating the dynamic management of listed drugs on the PBS. This amendment adds two new drugs, ivosidenib and maribavir, to the F1 formulary from 1 July 2025, while removing hypromellose with carbomer 980 from the F2 formulary as it will cease to be listed on the PBS. The Pharmaceutical Benefits Advisory Committee (PBAC) provided recommendations on these changes, ensuring that decisions about drug listing and formulary placement are evidence-based and aligned with clinical needs. This legislative instrument is designed to maintain the integrity of the PBS by ensuring that drugs are appropriately priced and accessible, while also protecting human rights by facilitating access to essential health care services.

Scope and Application

The National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 6) 2025 amends the National Health (Listed Drugs on F1 or F2) Determination 2021, which pertains to the allocation of drugs to the F1 and F2 formularies of the Pharmaceutical Benefits Scheme (PBS) under the National Health Act 1953. This instrument applies to pharmaceutical companies and other entities involved in the listing and supply of drugs under the PBS, particularly those affected by the changes in the formulary allocations. The amendments commence on 1 July 2025, impacting the availability and pricing of certain drugs by adding ivosidenib and maribavir to F1 and removing hypromellose with carbomer 980 from F2. The changes are made pursuant to the authority granted under the National Health Act and are subject to the criteria specified in the Act for drugs to be placed on F1 or F2. The amendments also consider recommendations from the Pharmaceutical Benefits Advisory Committee, ensuring decisions about PBS listings are evidence-based and aimed at improving access to essential medicines.

Key Provisions

The key provisions of the National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 6) 2025 (PB 79 of 2025) are contained within sections that amend the National Health (Listed Drugs on F1 or F2) Determination 2021 (PB 33 of 2021). This amendment introduces changes to the allocation of drugs within the Pharmaceutical Benefits Scheme (PBS) formularies F1 and F2. Specifically, two new drugs, ivosidenib and maribavir, are added to F1 effective from 1 July 2025, while the drug hypromellose with carbomer 980 is removed from F2 because it will no longer be listed on the PBS from the same date. These changes are made under the authority of subsection 85AB(1) of the National Health Act 1953, which allows the Minister or their delegate to determine by legislative instrument the allocation of drugs to the F1 or F2 formularies. The obligations imposed by this Act on the parties and entities it governs primarily concern the Pharmaceutical Benefits Advisory Committee (PBAC) and the responsible persons, which include pharmaceutical companies. The PBAC must review and provide recommendations on the inclusion of drugs on the PBS, ensuring that the decisions are evidence-based and in line with the principles of cost-effectiveness and clinical importance. Pharmaceutical companies are required to submit detailed consultations and submissions to the PBAC for any new drug they wish to have listed on the PBS. Additionally, the Minister or their delegate has the obligation to consider the PBAC’s recommendations and make a determination regarding the allocation of drugs to the appropriate formularies. The determination of this Act also outlines the consequences for breaches, although specific offences, penalties, or civil/criminal consequences are not detailed within the explanatory statement. Under the general legislative framework of the National Health Act 1953, non-compliance with the provisions of the Act could potentially lead to administrative actions, fines, or other penalties as prescribed by relevant laws. However, the explanatory statement does not provide explicit details on the maximum penalties for breaches related to this particular amendment. The overarching intent of the Act is to ensure that the PBS remains a sustainable and effective scheme for providing subsidised access to essential medicines while maintaining the highest standards of health care for Australians.

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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.