EXPLANATORY STATEMENT
INSTRUMENT NUMBER PB 110 OF 2009
NATIONAL HEALTH ACT 1953
AMENDMENT DETERMINATION UNDER SECTION 85B
Purpose and operation
Part VII of the National Health Act 1953 (the Act) is the legislative basis of the Pharmaceutical Benefits Scheme (PBS) by which the Commonwealth provides reliable, timely, and affordable access to a wide range of medicines for all Australians.
Subsection 85(1) provides that benefits are to be provided by the Commonwealth in accordance with Part VII in respect of pharmaceutical benefits.
Drugs and medicinal preparations to which Part VII applies are (with the exception of some medicinal preparations with additives) declared by the Minister by legislative instrument to be so under subsection 85(2). These are listed drugs as defined in subsection 84(1).
The Minister by legislative instrument can determine the form or forms of a listed drug by reference to strength, type of unit, size of unit or otherwise (subsection 85(3)); the manner of administration of the form of the listed drug so determined (subsection 85(5)); and a brand of the pharmaceutical item (defined in subsection 84(1)) that has the listed drug in that form with that manner of administration (subsection 85(6)). These determinations govern what constitutes the pharmaceutical benefit (defined in subsection 84(1)) under Part VII of the Act. Under section 84AF, the Minister may determine a responsible person for a brand of a pharmaceutical item.
Subsection 85B(1) provides that the section applies if the Minister and the responsible person for a brand of pharmaceutical item have been unable to make a price agreement under section 85AD on an amount that is to be taken to be the appropriate maximum price for sales of the brand of pharmaceutical item to approved pharmacists.
Under subsection 85B(2), the Minister may by legislative instrument determine, by reference to a quantity or number of units of a pharmaceutical item, the amount that is taken to be the appropriated maximum price for sales of the brand of the pharmaceutical item to pharmacists.
Under subsection 85B(3), the Minister may by legislative instrument determine, by reference to a quantity or number of units, the amount that is taken to be the price claimed by the responsible person as the responsible person’s price for sales of the brand of the pharmaceutical item to approved pharmacists.
Subsection 85B(4) provides the special patient contribution for the brand of the pharmaceutical item is the difference between the “responsible person’s Commonwealth price” and the “Commonwealth price” for the brand of the pharmaceutical item. Subsection 85(6) defines these terms to the effect that the Special Patient Contribution is the difference between the Commonwealth price (worked out in accordance with the determination of the Pharmaceutical Benefits Remuneration Tribunal under subsection 98B(1)) based on the amount determined under subsection 85B(2) and what would be the Commonwealth price based on the amount determined under subsection 85B(3).
Under subsection 85B(5), the Minister having made a determination under subsection 85B(3) may by legislative instrument determine the circumstances in which the Commonwealth is to pay the special patient contribution for the brand of the pharmaceutical item.
This legislative instrument in giving effect to recommendations of the Pharmaceutical Benefits Advisory Committee (PBAC) amends the determination under section 85B made by legislative instrument number PB 118 of 2008 which came into effect on 1 December 2008.
The amendment provides for changes to the price claimed (claimed price) by the responsible person for a brand of a pharmaceutical item and the Commonwealth agreed price (determined price) for the pharmaceutical item. The difference between the price claimed by the responsible person and the determined price forms the basis of a special patient contribution.
The amendment also provides for the deletion of brands of pharmaceutical items where a special patient contribution no longer applies.
The amendments are set out in the items of Schedule 1 to the instrument.
A provision-by-provision description of the instrument is contained in the Attachment.
This instrument, expressed to commence on 1 December 2009, was made on 12 November 2009.
Consultations
This instrument affects certain responsible persons with medicines listed on the PBS. If the Minister and responsible person cannot enter into a price agreement, consultation occurs between the responsible person and the Commonwealth and thereafter the Minister determines the price in relation to the relevant brand of pharmaceutical item and determines the price claimed by the responsible person as the responsible person's price for sales of the brand of pharmaceutical item to approved pharmacists.
ATTACHMENT
Paragraph 1: provides that this instrument commences on 1 December 2009.
Paragraph 2: provides that Schedule 1 amends PB 118 of 2008.
Schedule 1: provides for the following amendments:
SCHEDULE 1
Brands with an increased brand premium | ||
Allopurinol | Tablet 100 mg | Zyloprim |
| Tablet 300 mg | Zyloprim |
Betamethasone | Cream 200 micrograms (as valerate) per g, 100 g | Betnovate 1/5 |
| Cream 500 micrograms (as valerate) per g, 15 g | Betnovate 1/2 |
| Ointment 500 micrograms (as valerate) per g, 15 g | Betnovate 1/2 |
Digoxin | Tablet 62.5 micrograms | Lanoxin-PG |
| Tablet 250 micrograms | Lanoxin |
Glyceryl Trinitrate | Tablets 600 micrograms, 100 | Anginine Stabilised |
Hydrocortisone | Cream containing hydrocortisone acetate 10 mg per g, 30 g | Sigmacort |
| Cream containing hydrocortisone acetate 10 mg per g, 50 g | Sigmacort |
| Ointment containing hydrocortisone acetate | Sigmacort |
| Ointment containing hydrocortisone acetate | Sigmacort |
Levonorgestrel with Ethinyloestradiol | Tablets 150 micrograms-30 micrograms, 21 Pack containing 21 tablets 150 micrograms- | Microgynon 30 Microgynon 30 ED |
| Pack containing 6 tablets 50 micrograms- | Triquilar ED |
Minocycline | Tablet 50 mg (as hydrochloride) | Minomycin-50 |
Omeprazole | Tablet 20 mg (as magnesium) | Losec Tablets |
Ondansetron | I.V. injection 4 mg (as hydrochloride dihydrate) in | Zofran |
| I.V. injection 8 mg (as hydrochloride dihydrate) in | Zofran |
Oxazepam | Tablet 15 mg | Serepax |
| Tablet 30 mg | Serepax |
Pravastatin | Tablet containing pravastatin sodium | Pravachol |
| Tablet containing pravastatin sodium 80 mg | Pravachol |
Quinapril | Tablet 20 mg (as hydrochloride) | Accupril |
Thyroxine | Tablet containing 50 micrograms anhydrous thyroxine sodium | Oroxine |
| Tablet containing 75 micrograms anhydrous thyroxine sodium | Oroxine |
| Tablet containing 100 micrograms anhydrous thyroxine sodium | Oroxine |
| Tablet containing 200 micrograms anhydrous thyroxine sodium | Oroxine |
Trandolapril | Capsule 500 micrograms | Gopten |
| Capsule 1 mg | Gopten |
| Capsule 2 mg | Gopten |
| Capsule 4 mg | Gopten |
Triamcinolone | Cream containing triamcinolone acetonide | Aristocort 0.02% |
| Ointment containing triamcinolone acetonide | Aristocort 0.02% |
Trimethoprim | Tablet 300 mg | Triprim |
Trimethoprim with sulfamethoxazole | Tablet 160 mg-800 mg Paediatric oral suspension 40 mg-200 mg per 5 mL, 100 mL | Septrin Forte Septrin |
Brands with a price change but no change in brand premium | ||
Pravastatin | Tablet containing pravastatin sodium 10 mg | Pravachol |
| Tablet containing pravastatin sodium 40 mg | Pravachol |
Quinapril | Tablet 5 mg (as hydrochloride) | Accupril |
| Tablet 10 mg (as hydrochloride) | Accupril |
Brands which no longer have a brand premium | ||
Cefotaxime | Powder for injection 1 g (as sodium) | Cefotaxime Sandoz |
| Powder for injection 2 g (as sodium) | Cefotaxime Sandoz |
Cimetidine | Tablet 200 mg | Tagamet |
Potassium Chloride with Potassium Bicarbonate | Tablet, effervescent, 14 mmol potassium and 8 mmol chloride | Chlorvescent |
Quinine | Tablet containing quinine sulfate 300 mg | Quinate |