National Health (Listed drugs on F1 or F2) Amendment Determination (No. 5) 2026

Administered by Department of Health, Disability and Ageing

Legislation au F2026L00639 In force Legislative Instrument

Legislation content

EXPLANATORY STATEMENT

 

National Health Act 1953

 

National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 5) 2026

 

PB 63 of 2026

 

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 moving three currently listed drugs, febuxostat, ferric carboxymaltose and mifepristone and misoprostol from F1 to F2. In addition, two drugs, soy lecithin and toremifene are being removed from F1 as these drugs will no longer be PBS listed from 1 June 2026.

 

 

 

 

 

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. 

Febuxostat, ferric carboxymaltose and mifepristone and misoprostol no longer meet the criteria for F1 set out in section 85AB(4) of the Act so are required to be moved to F2 under subsection 85AB(3). The drugs, soy lecithin and toremifene are being removed from F1 as these drugs will no longer be listed on the PBS.

 

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 June 2026.

 

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. 5) 2026
(PB 63 of 2026)

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 moving three currently listed drugs, febuxostat, ferric carboxymaltose and mifepristone and misoprostol from F1 to F2. In addition, two drugs, soy lecithin and toremifene are being removed from F1 as these drugs will no longer be PBS listed from 1 June 2026.

 

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. 5) 2026, made under the National Health Act 1953, amends the National Health (Listed Drugs on F1 or F2) Determination 2021. This amendment involves the reallocation of certain drugs within the Pharmaceutical Benefits Scheme (PBS) formularies. Specifically, it moves febuxostat, ferric carboxymaltose, and mifepristone and misoprostol from F1 to F2, and removes soy lecithin and toremifene from F1 due to their removal from the PBS listing as of 1 June 2026. This legislative instrument, issued by the Australian government, aims to ensure that drugs are placed in formularies that reflect their therapeutic characteristics and market status, thereby facilitating efficient and cost-effective access to medications for patients. The amendments are made following consultations with pharmaceutical companies and recommendations from the Pharmaceutical Benefits Advisory Committee, which ensures evidence-based decision-making regarding drug subsidies.

Scope and Application

The National Health (Listed Drugs on F1 or F2) Amendment Determination (No. 5) 2026, made under the National Health Act 1953, 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). This legislative instrument applies to pharmaceutical companies and their listed drugs that are subject to the PBS. The amendment involves moving certain drugs from the F1 formulary to the F2 formulary, reflecting changes in their therapeutic status and availability. The changes are effective from 1 June 2026 and apply nationally across Australia. The Act does not specify exclusions or thresholds but relies on criteria for drug classification under the PBS, ensuring that the most cost-effective pricing and supply of medicines are maintained. The instrument is compatible with human rights, ensuring access to essential health care and social security as outlined in the International Covenant on Economic, Social and Cultural Rights.

Key Provisions

The main operative sections of this amendment to the National Health (Listed Drugs on F1 or F2) Determination 2021 (subsection 85AB(1) of the National Health Act 1953) focus on the reallocation of certain drugs from F1 to F2 formularies within the Pharmaceutical Benefits Scheme (PBS). Specifically, the amendment involves moving febuxostat, ferric carboxymaltose, and mifepristone and misoprostol from F1 to F2, while also removing soy lecithin and toremifene from F1 as they will no longer be listed on the PBS (section 85AB(3) and (4)). The F1 formulary is reserved for drugs with a single brand, while F2 is for drugs with multiple brands or those in a therapeutic group with other multi-brand drugs. This amendment ensures that the drugs are subject to the appropriate pricing and supply provisions under the Act. The obligations imposed by this Act on the parties or entities it governs include ensuring that the Pharmaceutical Benefits Advisory Committee (PBAC) makes evidence-based recommendations regarding the listing and formulary allocation of drugs on the PBS. Pharmaceutical companies must consult with the responsible person and submit recommendations to the PBAC, which consists of experts from various relevant fields. The Act also requires that any changes to the formulary allocation of drugs on the PBS are made through legislative instruments, ensuring transparency and accountability in the decision-making process. Failure to comply with the provisions of the Act may result in civil or criminal consequences. While the Act does not specify maximum penalties for non-compliance, any breaches of the legislative instrument or determinations made under it could potentially lead to legal action. Additionally, pharmaceutical companies may face reputational damage and financial losses if their drugs are not listed or allocated to the appropriate formulary on the PBS, as this could affect their marketability and profitability. The Act aims to ensure that decisions about drug listings and formulary allocations on the PBS are evidence-based and in the best interest of patients and the broader community.

Legal classification tags

Area of Law
Health Law
Pharmaceutical Law
Instrument
Legislative Instrument
Concepts
Definitions & Interpretation
Regulatory Standards
Reporting & Disclosure Obligations
Enforcement Powers

Interactions

Authorises

All Versions

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.