New Zealand Gazette – 1999 – No. 45

Page 1075

✨ Medicines Distribution Consents

15 APRIL NEW ZEALAND GAZETTE 1075

Note: This consent is valid for 2 years from the date of publication of this notice.

Dated this 7th day of April 1999.

G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.

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Consent to the Distribution of a New Medicine

Pursuant to section 20 of the Medicines Act 1981, the Minister of Health hereby consents to the distribution in New Zealand of the new medicine set out in the Schedule hereto:

Schedule

Name and Strength	Form	Name and Address of Manufacturer	Proprietary Name (if any)
Budesonide 1 mg/mL	Spray, nasal suspension	Douglas Pharmaceuticals Limited, Henderson, Auckland	Amcal Budesonide Nasal Spray
Pholcodine 0.2% w/v	Linctus	Douglas Pharmaceuticals Limited, Mount Wellington, Auckland	Amcal Cough Suppressant Double Strength
Pholcodine 0.1% w/v	Linctus	Douglas Pharmaceuticals Limited, Mount Wellington, Auckland	Amcal Cough Suppressant Regular Strength
Choline theophyllinate 1.5% guaiphenesin 0.75% w/v	Syrup	Douglas Pharmaceuticals Limited, Mount Wellington, Auckland	Amcal Expectorant Syrup
Paracetamol 24 mg/mL	Suspension, oral	Douglas Pharmaceuticals Limited, Mount Wellington, Auckland	Amcal Paracetamol Pain & Fever Relief
Paracetamol 500 mg	Tablet	Douglas Pharmaceuticals Limited, Henderson, Auckland	Amcal Paracetamol Pain Relief
Dolomite 400 mg	Tablet, chewable	Viminco A/S., Skaelskor, Denmark	Frutin
Paracetamol 2.4% w/v	Suspension, oral	PSM Healthcare Limited, Wiri, Auckland	Pharmacare Paramol Junior Suspension
Pholcodine 1 mg/mL	Linctus	PSM Healthcare Limited, Wiri, Auckland	Pholcodine Linctus
Pholcodine 2 mg/mL	Linctus	PSM Healthcare Limited, Wiri, Auckland	Pholcodine Strong Linctus

Dated this 7th day of April 1999.

G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.

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Consent to the Distribution of Changed Medicines

Pursuant to section 20 of the Medicines Act 1981, the Minister of Health hereby consents to the distribution of the changed medicines which were referred to the Minister of Health under the provisions of section 24 (5) of the Act and are set out in the Schedule hereto:

Schedule

Name and Strength	Form	Name and Address of Manufacturer	Proprietary Name (if any)
Filgrastim 300 µg/mL	Injection, powder	F Hoffmann-La Roche Limited, Basle, Switzerland; Parkedale Pharmaceuticals Inc., Rochester, Michigan, United States of America; and Amgen Inc., Juncos, Puerto Rico	Neupogen
Filgrastim 600 µg/mL	Injection, pre-filled syringe	F Hoffmann-La Roche Limited, Basle, Switzerland; and Parkedale Pharmaceuticals Inc., Rochester, Michigan, United States of America	Neupogen

Dated this 7th day of April 1999.

G. R. BOYD, Chief Advisor, Regulation and Safety, pursuant to delegation given by the Minister of Health on the 20th day of February 1997.

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VUW Te Waharoa — NZ Gazette 1999, No 45

NZLII — NZ Gazette 1999, No 45

The General Assembly Library (on the right) was completed in 1899 and survived the 1907 fire. Now the oldest remaining original Parliament building, still used as the Parliamentary Library.

✨ LLM interpretation of page content

🏥 Consent to the Distribution of a New Medicine

Domain🏥 Health & Social Welfare
Dated7 April 1999
KeywordsMedicines Act 1981, New Medicine, Provisional Consent, Distribution
👩‍💼 Officials

G. R. Boyd, Chief Advisor, Regulation and Safety

🏥 Consent to the Distribution of Changed Medicines

Domain🏥 Health & Social Welfare
Dated7 April 1999
KeywordsMedicines Act 1981, Changed Medicine, Distribution, Filgrastim
👩‍💼 Officials

G. R. Boyd, Chief Advisor, Regulation and Safety

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