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.