National Health Act 1953 - Determinations under sections 93 and 93aa - Pharmaceutical benefits supplied by medical practitioners and authorised nurse practitioners (No. PB 103 of 2010) (Cth)
PB 103 of 2010
Determinations — Pharmaceutical benefits supplied by medical practitioners and authorised nurse practitioners
as amended
made under sections 93 and 93AA of the
National Health Act 1953
This compilation was prepared on 1 September 2012
taking into account amendments up to PB 62 of 2012
Prepared by the Office of Legislative Drafting and Publishing,
Attorney‑General’s Department, Canberra
Determinations — Pharmaceutical benefits supplied by medical practitioners and authorised nurse practitioners
1. Name of Instrument [see Note 1]
(a) The name of this Instrument is Determinations under sections 93 and 93AA of the National Health Act 1953.
(b) This Instrument may also be cited as “No. PB 103 of 2010”.
2. Commencement
This Instrument commences on 1 November 2010.
3. Repeal
Determination No. PB 57 of 2007 under section 93 of the National Health Act 1953, made on 24 July 2007 with effect from 1 August 2007 (as amended) is repealed.
4. Definitions
In this Instrument:
“Act” means the National Health Act 1953;
“authorised nurse practitioner” has the meaning given by subsection 84(1) of the Act.
5. Pharmaceutical benefits
A pharmaceutical benefit which has a listed drug in a form mentioned in the Schedule is a pharmaceutical benefit which a medical practitioner and an authorised nurse practitioner is authorised to supply.
6. Maximum quantity or number of units
The maximum quantity or number of units of a pharmaceutical benefit which may be obtained by a medical practitioner or authorised nurse practitioner in any period of one month is the quantity or number of units mentioned in the Schedule under the column “maximum quantity” for the listed drug in the form mentioned less the quantity or number of units of the pharmaceutical benefit previously obtained in accordance with sections 93 and 93AA of the Act and still in the possession of the medical practitioner or authorised nurse practitioner.
| THE SCHEDULE | |||||
| Pharmaceutical benefits for supply by medical practitioners and authorised nurse practitioners | |||||
| Listed Drug | Form (strength, type, size, etc.) | Maximum quantity | |||
| Adrenaline | Injection 1 mg (as acid tartrate) in 1 mL (1 in 1,000) | 5 | |||
| Atropine | Injection containing atropine sulfate 600 micrograms in 1 mL | 10 | |||
| Benztropine | Injection containing benztropine mesylate 2 mg in 2 mL | 5 | |||
| Benzylpenicillin | Powder for injection 600 mg (as sodium) | 10 | |||
| OR | |||||
| Procaine Penicillin | Injection 1.5 g in disposable syringe | 5 | |||
| Benzylpenicillin | Powder for injection 3 g (as sodium) | 1 | |||
| Chlorpromazine | Injection containing chlorpromazine hydrochloride 50 mg in 2 mL | 10 | |||
| OR | |||||
| Haloperidol | Injection 5 mg in 1 mL | 10 | |||
| Clonazepam | Oral liquid 2.5 mg per mL, 10 mL | 1 | |||
| Dexamethasone | Injection containing dexamethasone sodium phosphate equivalent to 4 mg dexamethasone phosphate in 1 mL | 5 | |||
| OR | |||||
| Hydrocortisone | Injection 100 mg (as sodium succinate) with 2 mL solvent | 2 | |||
| OR | |||||
| Hydrocortisone | Injection 250 mg (as sodium succinate) with 2 mL solvent | 1 | |||
| Diazepam | Injection 10 mg in 2 mL | 5 | |||
| Diphtheria and tetanus vaccine, adsorbed, diluted for adult use | Injection 0.5 mL in pre-filled syringe | 20 | |||
| Frusemide | Injection 20 mg in 2 mL | 5 | |||
| Glucagon | Injection set containing glucagon hydrochloride 1 mg (1 I.U.) and 1 mL solvent in disposable syringe | 1 | |||
| Glyceryl Trinitrate | Sublingual spray (pump pack) 400 micrograms per dose, 200 doses | 1 | |||
| Hyoscine | Injection containing hyoscine butylbromide 20 mg in 1 mL | 5 | |||
| Lignocaine | Injection containing lignocaine hydrochloride 100 mg in 5 mL | 5 | |||
| Metoclopramide | Injection containing metoclopramide hydrochloride 10 mg in 2 mL | 10 | |||
| OR | |||||
| Prochlorperazine | Injection containing prochlorperazine mesylate 12.5 mg in 1 mL | 10 | |||
| Morphine | Injection containing morphine sulfate 15 mg in 1 mL | 5 | |||
| OR | |||||
| Morphine | Injection containing morphine sulfate 30 mg in 1 mL | 5 | |||
| Naloxone | Injection containing naloxone hydrochloride 2 mg in 5 mL disposable injection set | 2 | |||
| Promethazine | Injection containing promethazine hydrochloride 50 mg in 2 mL | 10 | |||
| Salbutamol | Pressurised inhalation 100 micrograms (as sulfate) per dose, 200 doses (CFC-free formulation) | 1 | |||
| OR | |||||
| Salbutamol | Nebuliser solution 2.5 mg (as sulfate) in 2.5 mL single dose units, 30 | 1 | |||
| Salbutamol | Nebuliser solution 5 mg (as sulfate) in 2.5 mL single dose units, 30 | 1 | |||
| Terbutaline | Injection containing terbutaline sulfate 500 micrograms in 1mL | 5 | |||
| Tramadol | Injection containing tramadol hydrochloride 100 mg in 2 mL | 5 | |||
| Verapamil | Injection containing verapamil hydrochloride 5 mg in 2 mL | 5 | |||
Notes to the Determinations — Pharmaceutical benefits supplied by medical practitioners and authorised nurse practitioners (PB 103 of 2010)
Note 1
The Determinations — Pharmaceutical benefits supplied by medical practitioners and authorised nurse practitioners (PB 103 of 2010) (in force under subsections 93 and 93AA of the National Health Act 1953) as shown in this compilation is amended as indicated in the Tables below.
Table of Instruments
| Title | Date of FRLI registration | Date of | Application, saving or |
| PB 103 of 2010 | 29 Oct 2010 (see F2010L02861) | 1 Nov 2010 | |
| PB 110 of 2010 | 30 Nov 2010 (see F2010L03135) | 1 Dec 2010 | — |
| PB 32 of 2011 | 13 Apr 2011 (see F2011L00606) | 1 May 2011 | — |
| PB 62 of 2012 | 15 Aug 2012 (see F2012L01681) | 1 Sept 2012 | — |
Table of Amendments
| ad. = added or inserted am. = amended rep. = repealed rs. = repealed and substituted | |
| Provision affected | How affected |
| Schedule | |
| Schedule.................................. | am. PB 110 of 2010; PB 32 of 2011; PB 62 of 2012 |
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