PB 26 of 2014

National Health (Weighted average disclosed price – supplementary disclosure cycle A) Determination 2014

National Health Act 1953

I, FELICITY MCNEILL, First Assistant Secretary, Pharmaceutical Benefits Division, Department of Health, delegate of the Minister for Health, make this determination under subsection 99ADB(4) and paragraph 99ADH(1)(aa) of the National Health Act 1953.

Dated: 14 April 2014

 

 

 

 

 

 

 

 

 

FELICITY MCNEILL

 

First Assistant Secretary

Pharmaceutical Benefits Division

Department of Health

 

1 Name of Determination

 (1) This Determination is the National Health (Weighted average disclosed price supplementary disclosure cycle A) Determination 2014.

 (2) This Determination may also be cited as PB 26 of 2014.

2 Commencement

  This Determination commences on the day after it is registered.

 

3                             Revocation

  This Determination revokes:

(a)                  the National Health (Weighted average disclosed price – supplementary disclosure cycle A) Determination 2013 (PB 24 of 2013);

(b)                  the National Health (Weighted average disclosed price – supplementary disclosure cycle B) Determination 2013 (PB 55 of 2013); and

(c)                  the National Health (Weighted average disclosed price – main disclosure cycle) Determination 2013 (No. 2) (PB 82 of 2013);

4                             Definitions

In this Determination:

 

Act means the National Health Act 1953.

 

adjusted approved ex-manufacturer price has the same meaning as in subsection 99ADB(1) of the Act.

 

supplementary disclosure cycle A has the same meaning as in regulation 37EB(2)(c) of the National Health (Pharmaceutical Benefits) Regulations 1960.

 

unadjusted price reduction has the same meaning as in subsection 99ADB(1) of the Act. 

                weighted average disclosed price has the same meaning as in subsection 99ADB(1) of the Act.

 

 

5                             Weighted average disclosed price for brands of pharmaceutical items – unadjusted price reduction is at least 10%

 

For subsection 99ADB(4) of the Act, the weighted average disclosed price specified in column 3 of an item in Schedule 1 is the weighted average disclosed price for the brand of pharmaceutical item specified in column 2 of the same item in Schedule 1.


6                             Weighted average disclosed price for brands of pharmaceutical items – unadjusted price reduction is less than 10%

 

For subsection 99ADB(4) of the Act, the weighted average disclosed price specified in column 3 of an item in Schedule 2 is the weighted average disclosed price for the brand of pharmaceutical item specified in column 2 of the same item in Schedule 2.

 

 

7                             Adjusted approved ex-manufacturer price for brands of pharmaceutical items – unadjusted price reduction is at least 10%

 

For paragraph 99ADB(4) of the Act, the adjusted approved ex-manufacturer price for a brand of pharmaceutical item specified in column 2 of Schedule 1 is an amount equal to the amount of the weighted average disclosed price of that brand of pharmaceutical item determined under section 5 of this instrument.

 

 

8                             Reduction Day

 

For paragraph 99ADH(1)(aa) of the Act, a brand of pharmaceutical item in the supplementary disclosure cycle A with a data collection period ending at the end of
31 January 2014 which is mentioned in Schedule 1 or 2 has a reduction day of
1 August 2014.

 

Schedule 1    

Brands of pharmaceutical items – unadjusted price reduction is at least 10%

 

Column 1

Column 2

Column 3

Item

Brand of Pharmaceutical Item

Weighted average disclosed price

 

Drug

Form

Manner of administration

Brand

 

1

Riluzole

Tablet 50 mg

Oral

APO-Riluzole

396.89

2

Riluzole

Tablet 50 mg

Oral

Rilutek

396.89

3

Riluzole

Tablet 50 mg

Oral

Riluzole Sandoz

396.89

Schedule 2    

Brands of pharmaceutical items – unadjusted price reduction is less than 10%

 

Column 1

Column 2

Column 3

Item

Brand of Pharmaceutical Item

Weighted average disclosed price

 

Listed Drug

Form

Manner of administration

Brand

 

1

Amlodipine with valsartan

Tablet 10 mg (as besylate)-160 mg

Oral

Exforge 10/160

17.84

2

Amlodipine with valsartan

Tablet 10 mg (as besylate)-320 mg

Oral

Exforge 10/320

20.92

3

Amlodipine with valsartan

Tablet 5 mg (as besylate)-160 mg

Oral

Exforge 5/160

14.99

4

Amlodipine with valsartan

Tablet 5 mg (as besylate)-320 mg

Oral

Exforge 5/320

18.08

5

Amlodipine with valsartan

Tablet 5 mg (as besylate)-80 mg

Oral

Exforge 5/80

12.53

6

Amlodipine with valsartan

Tablet 5 mg (as besylate)-80 mg

Oral

Valsartan/Amlodipine Sandoz 80/5

12.53

7

Amlodipine with valsartan and hydrochlorothiazide

Tablet 10 mg (as besylate)-160 mg-12.5 mg

Oral

Exforge HCT 10/160/12.5

19.26

8

Amlodipine with valsartan and hydrochlorothiazide

Tablet 10 mg (as besylate)-160 mg-25 mg

Oral

Exforge HCT 10/160/25

20.66

9

Amlodipine with valsartan and hydrochlorothiazide

Tablet 10 mg (as besylate)-320 mg-25 mg

Oral

Exforge HCT 10/320/25

23.76

10

Amlodipine with valsartan and hydrochlorothiazide

Tablet 5 mg (as besylate)-160 mg-12.5 mg

Oral

Exforge HCT 5/160/12.5

16.41

11

Amlodipine with valsartan and hydrochlorothiazide

Tablet 5 mg (as besylate)-160 mg-12.5 mg

Oral

Valsartan/Amlodipine/HCT Sandoz 160/5/12.5

16.41

12

Amlodipine with valsartan and hydrochlorothiazide

Tablet 5 mg (as besylate)-160 mg-25 mg

Oral

Exforge HCT 5/160/25

17.82

13

Imiquimod

Cream 50 mg per g, 2 g, 2

Application

Aldara Pump

102.57

14

Imiquimod

Cream 50 mg per g, 250 mg single use sachets, 12

Application

Aldara

102.57

15

Imiquimod

Cream 50 mg per g, 250 mg single use sachets, 12

Application

APO-Imiquimod

102.57

16

Nevirapine

Tablet 200 mg

Oral

Nevirapine Alphapharm

215.24

17

Nevirapine

Tablet 200 mg

Oral

Nevirapine RBX

215.24

18

Nevirapine

Tablet 200 mg

Oral

Viramune

215.24

19

Nevirapine

Tablet 400 mg (extended release)

Oral

Viramune XR

215.24

Note

1. All legislative instruments and compilations are registered on the Federal Register of Legislative Instruments kept under the Legislative Instruments Act 2003. See http://www.comlaw.gov.au.