National Health (Price and Special Patient Contribution) Amendment Determination 2011 (No. 5) (No. PB 50 of 2011)

Administered by Department of Health, Disability and Ageing

Legislation au F2011L01546 Not in force Legislative Instrument

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EXPLANATORY STATEMENT

National Health Act 1953

National Health (Price and Special Patient Contribution)

Amendment Determination 2011 (No. 5)

PB 50 of 2011

 

Purpose

This legislative instrument amends the National Health (Price and Special Patient Contribution) Determination 2010 ( PB 109 of 2010) which provides for price determinations in relation to brands of pharmaceutical items for which the Minister and the responsible person have not been able to make a price agreement.  The Determination is made under section 85B of the National Health Act 1953 (the Act).  The amendment amends Schedule 1 of PB 109 of 2010. 

Background – the Pharmaceutical Benefits Scheme

Part VII of the Act is the legislative basis of the Pharmaceutical Benefits Scheme (PBS) under which the Commonwealth provides reliable, timely, and affordable access to a wide range of medicines for all Australians.

Subsection 85(1) provides that pharmaceutical benefits are to be provided by the Commonwealth in accordance with Part VII.

In the case of ready-prepared pharmaceutical benefits, the pharmaceutical benefit is a brand of a pharmaceutical item.  That is, it is a brand of a listed drug, in a form and with a manner of administration, declared and determined under various provisions of Part VII.

Part VII also provides for numerous other matters, including pricing matters and matters relating to payments by the Commonwealth and charges to patients for pharmaceutical benefits.  This Determination concerns such matters.

Background – the Determination

The Act provides for the Minister and the responsible person to agree a price that is taken to be the appropriate maximum price for sales of a brand of a pharmaceutical item to approved pharmacists (section 85AD).  Section 85B of the Act applies if the Minister and the responsible person have been unable to reach an agreement.

Subsection 85B(2) provides that the Minister may determine an amount that is taken to be the appropriate maximum price for sales of a brand of a pharmaceutical item to approved pharmacists.  This is termed the ‘Determined Price’.

Subsection 85B(3) provides that the Minister may determine an amount that is taken to be the price claimed by the responsible person as the appropriate maximum price for sales of the brand of the pharmaceutical item to approved pharmacists.  This is termed the ‘Claimed Price’.

The Determined Price is the approved price to pharmacists and is used as the basis for working out the Commonwealth price for the brand of the pharmaceutical item (section 98B of the Act).  Approved pharmacists are entitled to payment from the Commonwealth equal to the Commonwealth price less the applicable patient co-payment (section 99 of the Act).

The difference between the responsible person’s Commonwealth price (ie, the price that would be the Commonwealth price if the responsible person’s claimed price had become the approved price to pharmacists) and the Commonwealth price for the brand is defined in subsection 85B(4) of the Act as the special patient contribution.  An approved pharmacist may charge a patient an amount equal to the special patient contribution, in addition to any other amount that may be charged (subsection 87(2A) of the Act).

Subsection 85B(5) of the Act provides that the Minister may determine the circumstances in which the Commonwealth is to pay the special patient contribution for a brand.  In such cases the Commonwealth payment to the pharmacist is increased by the amount of the special patient contribution (subsection 99(2AA) of the Act) and the pharmacist may not charge the patient this amount (subsection 87(2A) of the Act). 

The purpose of making subsection 85B(5) determinations is to enable patients for whom the base-priced brands (the ones without a special patient contribution) are not suitable, to obtain the higher priced brand (the one with the special patient contribution) without the need to pay the higher price.  In such cases the Commonwealth pays the special patient contribution.

This Determination contains determinations of:

  • Determined Prices (under subsection 85B(2) of the Act);
  • Claimed Prices (under subsection 85B(3) of the Act); and

 

Changes effected by this Determination

A provision-by-provision description of this instrument is contained in Attachment 1.

This instrument amends PB 109 of 2010 by amending Schedule 1, Determined and Claimed Prices. 

The effect of the Schedule 1 amendments is to remove one brand of the pharmaceutical item bromocriptine in the pack sizes of 30 and 60. It also shows the increase and decrease to existing pharmaceutical items, including a pharmaceutical item that has a therapeutic group premium and inserts a new pharmaceutical item sumatriptan.  

The changes made in this instrument to matters determined under section 85B of the Act since the last amendment made on 1 July 2011, are set out in Attachment 2 to this Explanatory Statement and is titled Summary of Changes.


Consultation

This determination affects certain responsible persons with medicines listed on the PBS.  Before a pharmaceutical benefit is listed on the PBS, and from time to time thereafter, price negotiations occur between the responsible person and the Minister for the purpose of reaching a price agreement for section 85AD of the Act.  If the Minister and the responsible person cannot agree on a price, further consultation occurs with the responsible person, and thereafter the Minister determines the price that will be the approved price to pharmacists for the brand.  The Minister also determines the corresponding price claimed by the responsible person which is used to calculate the special patient contribution that will apply to the brand. 

 

The Determination

A provision by provision description of the Determination is contained in Attachment 1.

The Amendment Determination commences on 1 August 2011. 

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

ATTACHMENT 1

 

PROVISION BY PROVISION DESCRIPTION OF THE AMENDMENT DETERMINATION

 

Section 1   Name of Determination

This section provides that this Determination is the National Health (Price and Special Patient Contribution) Amendment Determination 2011 (No. 5) and may also be cited as PB 50 of 2011.

Section 2   Commencement

This section provides that the Amendment Determination commences on                    1 August 2011.

Section 3   Amendment of PB 109 of 2010

This section provides that Schedule 1 of the Instrument amends the determination under section 85B of the Act the National Health (Price and Special Patient Contribution) Determination 2010 (PB 109 of 2010).

Schedule 1   Amendments

Schedule 1 sets out the amendments to Determination PB 109 of 2010.


ATTACHMENT 2

 

SUMMARY OF CHANGES

SCHEDULE 1

 

Brands to which a brand premium no longer applies

Bromocriptine

Tablet 2.5 mg (as mesylate) [Quantity or Number of
Units 30]

Parlodel

 

Tablet 2.5 mg (as mesylate) [Quantity or Number of
Units 60]

Parlodel

 

Brand with new brand premium

Sumatriptan

Tablet 50 mg (as succinate)

Imigran

 

Brands with an increased brand premium

Amoxycillin with Clavulanic Acid

Tablet containing 500 mg amoxycillin (as trihydrate) with 125 mg clavulanic acid (as potassium clavulanate)

Augmentin Duo

 

Tablet containing 875 mg amoxycillin (as trihydrate) with 125 mg clavulanic acid
(as potassium clavulanate)

Augmentin Duo Forte

 

Powder for oral suspension containing 125 mg amoxycillin (as trihydrate) with 31.25 mg clavulanic acid (as potassium clavulanate) per 5 mL, 75 mL

Augmentin

 

Powder for oral suspension containing 400 mg amoxycillin (as trihydrate) with 57 mg clavulanic acid (as potassium clavulanate) per 5 mL, 60 mL

Augmentin Duo 400

Lamotrigine

Tablet 5 mg

Lamictal

 

Tablet 25 mg

Lamictal

 

Tablet 50 mg

Lamictal

 

Tablet 100 mg

Lamictal

 

Tablet 200 mg

Lamictal

Ranitidine

Tablet 150 mg (as hydrochloride)

Zantac

 

Tablet 300 mg (as hydrochloride)

Zantac

Tramadol

Capsule containing tramadol hydrochloride 50 mg

Tramal

 

Tablet (sustained release) containing tramadol hydrochloride 100 mg

Tramal SR 100

 

Tablet (sustained release) containing tramadol hydrochloride 150 mg

Tramal SR 150

 

Tablet (sustained release) containing tramadol hydrochloride 200 mg

Tramal SR 200

 

Brands with a price change and decreased brand premium

Escitalopram

Tablet 10 mg (as oxalate)

Lexapro

 

Tablet 20 mg (as oxalate)

Lexapro

Meloxicam

Tablet 7.5 mg

Mobic

 

Tablet 15 mg

Mobic

Methylprednisolone

Injection containing methylprednisolone acetate 40 mg in 1 mL

Depo-Medrol

Nifedipine

Tablet 10 mg

Adalat 10

 

Tablet 60 mg (controlled release)

Adalat Oros 60

Salbutamol

Pressurised inhalation 100 micrograms (as sulfate) per dose, 200 doses (CFC-free formulation)

Ventolin CFC-Free

Valproic Acid

Tablet (enteric coated) containing sodium valproate
200 mg

Epilim EC

 

Tablet (enteric coated) containing sodium valproate
500 mg

Epilim EC

Brands with a price change and an increased brand premium

Lercanidipine

Tablet containing lercanidipine hydrochloride 10 mg

Zanidip

 

Tablet containing lercanidipine hydrochloride 20 mg

Zanidip

 

Brands with a price change but no change in brand premium

Felodipine

Tablet 2.5 mg (extended release)

Plendil ER

 

Tablet 5 mg (extended release)

Plendil ER

 

Tablet 10 mg (extended release)

Plendil ER

Nifedipine

Tablet 20 mg

Adalat 20

 

Tablet 30 mg (controlled release)

Adalat Oros 30

 

Brand with a price change but no change in therapeutic group premium

Nifedipine

Tablet 20 mg (controlled release)

Adalat Oros 20

 

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