Pharmaceutical Benefits Regulations (Amendment) (Cth)

STATUTORY RULES.

1950. No. 94.

REGULATIONS UNDER THE PHARMACEUTICAL BENEFITS ACT 1947-1949.*

I

, THE GOVERNOR-GENERAL in and over the Commonwealth of Australia, acting with the advice of the Federal Executive Council, hereby make the following Regulations under the Pharmaceutical Benefits Act 1947-1949.

Dated this thirtieth day of November, 1950.

W. J. McKELL

Governor-General.

By His Excellency's Command,

EARLE PAGE

Minister of State for Health.

AMENDMENTS OF THE PHARMACEUTICAL BENEFITS REGULATIONS. 

Supply of benefits upon prescriptions.

1. Regulation 12 of the Pharmaceutical Benefits Regulations is amended—

(a) by omitting from sub-paragraph (ii) of paragraph (c)of sub-regulation (2.) the words "specified, in relation to the pharmaceutical benefit, in column 2 of Table A in the Third Schedule to these Regulations ";

(b) by inserting in sub-regulation (2.), after paragraph (c),the following paragraph :—

 " (ca)the prescription indicates the name and address of the person for whom the pharmaceutical benefit is to be supplied; " ; and

(c) byomitting from sub-regulation (4.) the words " specified, in relation to the pharmaceutical benefit, in column 2 of Table A in the Third Schedule to these Regulations ".

Prescribing of certain drugs restricted.

2. Regulation 14 of the Pharmaceutical Benefits Regulations is amended—

(a) by omitting sub-regulation (1.) and inserting in its stead the following sub regulation : ─

" (1.) A medical practitioner shall not write on an authorized prescription form a prescription for the supply of a pharmaceutical benefit to which this regulation applies unless”—

(a) the Director-General or a delegate of the Director-General has given to him a numbered authority so to write the prescription; and

* Notified in the Commonwealth Gazette on 30th November, 1950.

  Statutory Rules 1950, No. 48, as amended by Statutory Rules 1950, Nos. 51, 55 and 62.

5894.—PRICE 5D.

(b) he refers, on the form, to that authority and its number." ; and

(b) by inserting in sub-regulation (2.), after the word " with ", the words " paragraph (b) of ".

Standards of purity.

3. Regulation 36 of the Pharmaceutical Benefits Regulations is repealed and the following regulation inserted in its stead :—

" 36. —(1.) A pharmaceutical benefit which is included in the British Pharmacopoeia shall conform to the standards of purity thereby required.

" (2.) A pharmaceutical benefit which is not included in the British Pharmacopoeia but is included in the British Pharmaceutical Codex shall conform to the standards of purity required by that Codex.".

Containers.

4. Regulation 37 of the Pharmaceutical Benefits Regulations is amended byomitting from sub-regulation (2.) the word and letter " Table B " and inserting in their stead the word and letter " Table A ".

Second Schedule.

5.—(1.) The Second Schedule to the Pharmaceutical Benefits Regulations is amended—

(a) by inserting after Item 32 the following Item :—

" 32A	DISTILLED WATER (Sterile)	................................	2 cc. amp..............................	6	1
................................	3 cc. amp.............................	6	1
................................	5 cc. amp.............................	6	1
................................	10 cc. amp.............................	6	1 " ;

(b) by omitting Item 65 and inserting in its stead the following Item :—

" 65	METHIONINE	................................	50 G. bottle .............................	1	..
................................	0.25 G. tab..............................	100	1
................................	0.5 G. tab..............................	100	1 " ;

(c) by inserting after Item 100 the following Item: —

" 100A PROTOLEX ................................ 10 cc. amp.............................. 1 1

(d) by inserting after Item 124 the following Item :—

" 124A	sulphonamides mixed (c)	................................	7 ½ gr. tab..............................	100	1 ";
Sulphadiazine 26 ⅔%	and
Sulphamerazine 26 ⅔%
Sulphanilamide 23 ⅓%
Sulphathiazole 23 ⅓%

(e) in accordance with the Schedule to these Regulations.

(2.) In the Schedule to these Regulations, " words " includes letters, figures and symbols.

Third Schedule.

6. The Third Schedule to the Pharmaceutical Benefits Regulations is amended-—

(a) by omitting paragraph 1;

(b) by omitting paragraph 3 and inserting in its stead the following paragraph :—

" 3.—(1.) Subject to this paragraph, the amount of the payment in respect of a pharmaceutical benefit supplied at a place in Zone 1 shall be the sum of the following amounts, as determined by the Director-General :—

(a)the wholesale cost, as at the first day of the month in which the supply took place, of the pharmaceutical benefit in the form and quantity in

 

which it was supplied and on the basis that it was supplied in or from the standard package, plus one-third of that cost ;

(b)where the number of units of the pharmaceutical benefit, as directed in the prescription to be supplied, was not the number, or a multiple of the number, contained in the standard package an amount, ascertained in the manner agreed on from time to time between the Commonwealth and the Federated Pharmaceutical Service Guild of Australia, as an allowance for wastage resulting from dividing the contents of the standard package and an amount for the supply of a container ascertained in accordance with Table A at the end of this Schedule ; and

(c) a dispensing fee-

(i) in the case of capsules, tablets and pills of fifteen pence ;

(ii) in the case of ampoules, vials and any other forms of fourteen pence.

" (2.) The amount of the payment in respect of a pharmaceutical benefit specified in any of items 58 to 61 (inclusive) in the Second Schedule to these Regulations supplied at a place in Zone 1 shall be the amount determined by the Director-General to be the retail price, as at the first day of the month in which the supply took place, of the pharmaceutical benefit in the form and quantity in which it was supplied.

" (3.) Where the prescription does not identify the form in which the pharmaceutical benefit is to be supplied by reference to a trade mark, brand or name used by a particular manufacturer, the pharmaceutical benefit shall, for the purposes of this paragraph, be deemed to have been supplied in a form in which the pharmaceutical benefit is available in the standard package, being a form in relation to which the wholesale cost of the standard package, as at the first day of the month in which the supply took place, was not higher than the wholesale cost, as at that date, of the standard package of the pharmaceutical benefit in any other form which was available to the supplier from a manufacturer.

" (4.) The amount of a payment under this paragraph shall be adjusted to the nearest penny, any odd half-penny being counted as one penny.

" (5.) In this paragraph, but subject to the next succeeding sub-paragraph, ' the standard package ', in relation to a pharmaceutical benefit, means—

(a) where there is supplied by one or more manufacturers of the pharmaceutical benefit package of the pharmaceutical benefit which

 

contains a number of units equal to the number specified in column 5 of the Second Schedule to these Regulations in relation to that pharmaceutical benefit a package containing that number of units ; or

(b) where such a package is not supplied by any manufacturer, but one or more manufacturers supply a package or packages containing a greater number of units than the number specified in column 5 of the Second Schedule to these Regulations in relation to the pharmaceutical benefit a package containing the least number of units contained in any of those packages ; and

(c) where the packages of the pharmaceutical benefit supplied by manufacturers all contain a lesser number of units than the number of units specified in relation to the pharmaceutical benefit in column 5 of the Second Schedule to these Regulations a package containing the greatest number of units contained in any of those packages.

" (6.) Where the prescription identifies the pharmaceutical benefit to be supplied by reference to a trade mark, brand or name used by a particular manufacturer, the standard package, for the purposes of this paragraph, shall be ascertained as if the pharmaceutical benefit were not supplied by any other manufacturer." ;

(c)by omitting all the words and figures from the beginning of paragraph 7 to the end of Table A ; and

(d) byomitting the heading " Table B " and inserting in its stead the heading " Table A ".

THE SCHEDULE.

Reg. 5.

AMENDMENTS TO SECOND SCHEDULE OF PRINCIPAL REGULATIONS.

Item No.	Amendments in Columns 3, 4, 5 and 6.
4	Before line 1 insert ─
“	.................................................	2 min. cap....................	12	3 ”
7	After line 3 insert ─
“	1/100 gr. per cc.........................	10 cc. vial ...................	1	.. ”
18	Omit all words, insert ─
“	5% ...........................................	1,000 cc. bottle ............	1	..
5% ...........................................	500 cc. bottle ..............	1	..
“	2 ½% .......................................	500 cc. bottle ..............	1	.. "
22	Add ─
8,000 M. per cc.........................	1 cc. amp.....................	2	.."
23	After line 3 insert ─
“	.................................................	50 mg. amp .................	1	..
.................................................	50 mg. crystule............	1	.."

 

THE SCHEDULE—continued.

AmendmentstosecondscheduleofPrincipalRegulations— continued.

Item No.	Amendments in Columns 3, 4, 5 and 6.
24	After line 2 insert—
"	...........................................	1/16 gr. hypo. tab.........	10	.. "
31	Add—
"	...........................................	3 cc. vial .....................	1	1 "
36	After line 1 insert—
"	½ gr. per cc. .......................	1 cc. amp. ...................	6	1 "
After line 3 insert—
"	...........................................	½ gr. hypo. tab.............	20	1 "
57	After line 3 insert—
"	1/100 gr. per cc. .................	10 cc. vial ...................	1	.. "
64	After line 5 insert—
"	10 U.S.P. U. per cc..............	10 cc. vial ...................	1	1 "
Omit line 7
71	After line 4 insert—
"	½ gr. per cc.........................	10 cc. vial....................	1	.. "
84	After line 1 insert—
"	1 gr. per 4 cc.......................	4 cc. amp. ...................	6	.. "
89	After line 3 insert—
"	10,000 M. per cc.................	5 cc. vial ....................	1	..
20,000 M. per cc.................	5 cc. vial ....................	1	..
50,000 M. per cc.................	5 cc. vial .....................	1	.. "
91	Omit from column 3 " 0.1 G. per cc. ”, insert " 0.1 G. per 2 cc."
95	After line 2 insert—
"	0.3% ..................................	20 cc. bottle ................	1	..
97	Omit all words, insert—
"	...........................................	300,000 U. amp. ..........	6	..
...........................................	400,000 U. amp...........	6	..
...........................................	600,000 U. amp...........	6	..
...........................................	900,000 U. amp. ..........	6	..
...........................................	1,200,000 U. amp.........	6	.. "
98	Omit all words insert—
"	...........................................	1 cc. amp. ...................	6	..
...........................................	1 cc. syrette .................	6	..
...........................................	300,000 U. amp...........	6	..
...........................................	10 cc. amp. .................	1	..
...........................................	600,000 U. amp...........	6	..
...........................................	1 million U. amp..........	6	..
...........................................	600,000 U. syrette........	6	..
...........................................	300,000 U. syringe ......	6	..
...........................................	600,000 U. syringe ......	6	.. "
107	Omit from column 5 figure " 2 " (wherever occurring), insert " 1 "   Omit from column 6 figure " 1 " (wherever occurring), insert " 3 "
108						Omit from column 5 figure " 2 " (wherever occurring), insert " 1 "
Omit from column 6 figure " 1 " (wherever occurring), insert " 3 "
109	After line 3 insert—
"	...........................................	20 cc. amp...................	6	1
...........................................	50 cc. amp...................	3	1 "
121	Omit all words
"	...........................................	5 gr. enseal  ................	100	1
...........................................	7½ gr. tab ....................	100	1 "
123	After line 1 insert—
"	...........................................	0.33 G. tab...................	100	1 "
124	Omit all words, insert—
"	...........................................	0.25 G. troche .............	100	1
...........................................	0.3 G. dulcet................	100	1
...........................................	0.5 G. tab.....................	100	1 "

5894.─2

THE SCHEDULE—continued.

AmendmentstoSecondScheduleofPrincipalRegulations— continued.

Item No.	Amendments in Columns 3, 4, 5 and 6.
128	After line 2 insert—
"		0.366 G. per 10 mil............		10 mil. amp.......................	6	.. "
After line 4 insert—
“		0.732 G. per 2 mil..............		2 mil. amp.........................	6	.. "
After line 5 insert—
“	.........................................			2.34 gr. Tab. .....................	100	1 "
132	After last line add—
“	.........................................			5 gr. tab. ...........................	100	3 "
137	After line 3 add—
“	100 γ per cc.......................			1 cc. amp...........................	1	1 "

By Authority : L. F. JOHNSTON, Commonwealth Government Printer, Canberra.