VALABARB

Main information

  • Trade name:
  • VALABARB EUTHANASIA SOLUTION
  • Pharmaceutical form:
  • PARENTERAL LIQUID/SOLUTION/SUSPENSION
  • Units in package:
  • 500mL
  • Class:
  • Veterinary Medicine
  • Medicine domain:
  • Animals
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • VALABARB EUTHANASIA SOLUTION
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • ANIMAL
  • Therapeutic area:
  • euthanasia
  • Therapeutic indications:
  • EUTHANASIA
  • Product summary:
  • For euthanasia only.FOR EUTHANASIA ONLY. NOT TO BE USED AS AN ANAESTHETIC. Not for use in animals intended for human or animal consumption.

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Registered and available
  • Authorization number:
  • 36208/55202
  • Authorization date:
  • 14-05-2012
  • Last update:
  • 15-06-2017

Patient Information leaflet: composition, indications, side effects, dosage, interactions, adverse reactions, pregnancy, lactation

V ala barb Euthanasia Solution

Relevant label particulars

27APR12

page 1/3

Bottle Label (500 mL amber

glass)-

Panel I

PRESCRIPTION ANIMAL REMEDY

KEEP OUT OF REACH OF CHILDREN

ANIMAL TREATMENT ONLY

VALABARB®

EUTHANASIA

SOLUTION

ACTIVE CONSTITUENT:

300 mg/mL PENTOBARBITONE SODIUM

(equivalent

mg/mL

PENTOBARBITONE)

FOR EUTHANASIA ONLY

NOT TO BE USED

AS AN ANAESTHETIC

use only by registered veterinary surgeons

practitione1·s

persons

authorised

under

relevant

State

Territory

legislation.

[jurox

logo]

SOOmL

Bottle Label (500 mL amber

glass)-

Panel2

DIRECTIONS

USE:

use only by registered

veterinary

surgeons

practitioners

persons

authorised

under

relevant

State

Territory

legislation.

Approved

Restraints:

animals

intended

human

animal

consumption.

Dosage

administration:

Administer by intravenous injection.

DOSE: 1-2 mL per 5 kg bodyweight.

FIRST AID

poisoning occurs, contact a doctor or Poisons Infmmation Centre. Phone Australia

Jurox Pty Limited

85 Gardiner Street, Rutherford NSW 2320 Australia

Infoline: 1800

DISPOSE

empty container by wrapping with paper and placing in garbage.

STORE below 30°C (Room Temperature).

Protect from light.

Infopest

Verified

Valabarb Euthanasia Solution

Relevant label particulars

27APR12

Bottle Label (500 mL amber

glass)-

Panel2

(cont.)

[Item code]

APVMA

36208/55202

EXP.

page 2/3

Bottle Label (100 mL, 200 mL, 250 mL, 500 ml

HDPE)-

Panell

PRESCRIPTION ANIMAL REMEDY

KEEP OUT

REACH

CHILDREN

ANIMAL TREATMENT ONLY

VALABARB®

EUTHANASIA

SOLUTION

ACTIVE CONSTITUENT:

mg/mL PENTOBARBITONE SODIUM

(equivalent

mg/mL

PENTOBARBITONE)

FOR EUTHANASIA ONLY

NOT TO BE USED

ANAESTHETIC

use only

registered veterinary surgeons

practitioners

persons

authorised

under

relevant State

Territory

legislation.

[jurox

logo]

[100] [200] [250] [500)

Bottle Label

00 mL, 200 mL, 250

500 ml HDPE)

-Panel

DIRECTIONS

USE:

use only by registered veterinary surgeons

practitioners

persons

authorised .

under

relevant State

Territory

legislation.

Restraints: DO NOT USE in animals intended for

human

animal consumption.

Dosage

administration: Administer

intravenous injection.

DOSE: 1-2 mL per 5 kg bodyweight.

Valabarb Euthanasia Solution

Relevant label pmiiculars

27APR12

page 3/3

Bottle Label (100 mL, 200 mL, 250

HDPE)-

Panel2

(cont.)

FIRST AID

poisoning occurs, contact a doctor or Poisons Information Centre. Phone Australia

Jurox Pty Limited

Gardiner Street, Rutherford NSW 2320 Australia

Infoline: 1800 023 312

DISPOSE

empty container by wrapping with paper and placing in garbage.

STORE below 30°C (Room Temperature).

Protect from light.

[Item code]

APVMA 36208/55202

EXP.

19-12-2018

Safety and efficacy of vitamin B2 (riboflavin 5′‐phosphate ester monosodium salt) for all animal species when used in water for drinking

Safety and efficacy of vitamin B2 (riboflavin 5′‐phosphate ester monosodium salt) for all animal species when used in water for drinking

Published on: Tue, 18 Dec 2018 Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on vitamin B2 in the form of riboflavin 5′‐phosphate ester monosodium salt as an additive for all animal species for use in water for drinking. The additive under assessment is obtained from ■■■■■ a source of riboflavin produced by Ashbya gossypii. No information was provided on the identity and character...

Europe - EFSA - European Food Safety Authority EFSA Journal

18-12-2018

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Torrance, CA, Asclemed USA Inc is voluntarily recalling 20 lots of Dyural-40 and 61 lots of Dyural-80, to the user level. The products include recalled Sodium Chloride, USP, 0.9% manufactured by Fresenius Kabi, which has been recalled due to product labeling incorrectly stating stoppers do not contain latex.

FDA - U.S. Food and Drug Administration

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Magnesium citrate malate as a source of magnesium added for nutritional purposes to food supplements

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21-11-2018

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FDA - U.S. Food and Drug Administration

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Safety and efficacy of Monimax® (monensin sodium and nicarbazin) for chickens for fattening and chickens reared for laying

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Europe - EFSA - European Food Safety Authority Publications

15-11-2018

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14-11-2018

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Health Canada

9-11-2018

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Europe - EFSA - European Food Safety Authority Publications

5-11-2018

Products containing metam-sodium: ANSES announces the withdrawal of marketing authorisations

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France - Agence Nationale du Médicament Vétérinaire

30-10-2018

Sciegen Pharmaceuticals, Inc. Issues Voluntary Nationwide Recall of Irbesartan Tablets, USP  75 Mg, 150 Mg, and 300 Mg Due to The Detection of Trace Amounts of NDEA (N-Nitrosodiethylamine) Impurity Found in The Active Pharmaceutical Ingredient (API)

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FDA - U.S. Food and Drug Administration

30-10-2018

Pest categorisation of Aleurocanthus spp.

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Europe - EFSA - European Food Safety Authority Publications

18-10-2018

Stewart’s Shops Issues Allergy Alert on Undeclared Milk in Cranberry Apple Refresher

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FDA - U.S. Food and Drug Administration

18-9-2018

Peer review of the pesticide risk assessment of the active substance sodium hydrogen carbonate

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12-9-2018

FDA takes new steps to address epidemic of youth e-cigarette use, including a historic action against more than 1,300 retailers and 5 major manufacturers for their roles perpetuating youth access

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FDA - U.S. Food and Drug Administration

7-9-2018

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7-9-2018

SCA Pharmaceuticals LLC. Issues Voluntary Nationwide Recall of Furosemide 100 mg in 0.9% Sodium Chloride due to Presence of Precipitate

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FDA - U.S. Food and Drug Administration

31-8-2018

FDA announces voluntary recall of Montelukast tablets by Camber Pharmaceuticals due to incorrect drug in bottles

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FDA - U.S. Food and Drug Administration

29-8-2018

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FDA - U.S. Food and Drug Administration

31-7-2018

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FDA - U.S. Food and Drug Administration

19-7-2018

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Europe - EFSA - European Food Safety Authority Press Releases & News Stories

18-7-2018

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Safety advisory - diabetic ketoacidosis and surgical procedures

Therapeutic Goods Administration - Australia

25-5-2018

Orphan designation:  Treprostinil sodium,  for the: Treatment of chronic thromboembolic pulmonary hypertension

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Europe - EMA - European Medicines Agency

17-5-2018

JAGUAR 30000 capsules

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Safety advisory

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19-12-2018

Macugen (PharmaSwiss CeskA republika s.r.o.)

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Europe -DG Health and Food Safety

18-12-2018


Calcium chloride / glutamic acid / glutathione / histidine / lactobionic acid / magnesium chloride / mannitol / potassium chloride / sodium hydroxide: List of nationally authorised medicinal products - PSUSA/00010390/201801

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Europe - EMA - European Medicines Agency

17-12-2018


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Europe - EMA - European Medicines Agency

14-12-2018


Referral: Fosfomycin-containing medicinal products, fosfomycin calcium, fosfomycin disodium, fosfomycin sodium, fosfomycin trometamol, Article 31 referrals, Procedure started, 13/12/2018

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Europe - EMA - European Medicines Agency

12-12-2018


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Europe - EMA - European Medicines Agency

12-12-2018


Magnesium sulphate heptahydrate, sodium sulphate anhydrous, potassium sulphate: List of nationally authorised medicinal products - EMEA/H/N/PSR/S/0016

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Europe - EMA - European Medicines Agency

10-12-2018

EU/3/17/1893 (SFL Regulatory Services GmbH)

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EU/3/17/1893 (Active substance: Polyphenyl(disodium 3-O-sulfo-beta-D-glucopyranuronate)-(1?3)-beta-D-galactopyranoside) - Transfer of orphan designation - Commission Decision (2018)8628 of Mon, 10 Dec 2018 European Medicines Agency (EMA) procedure number: EMA/OD/048/17/T/01

Europe -DG Health and Food Safety

3-12-2018


Withdrawn application: Zydax, glucuronoxylan sulfate sodium, Date of withdrawal: 03/12/2018, Initial authorisation

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Europe - EMA - European Medicines Agency

28-11-2018

PHEBURANE (Eurocept International BV)

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PHEBURANE (Active substance: Sodium Phenylbutyrate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)8043 of Wed, 28 Nov 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2500/T/20

Europe -DG Health and Food Safety

22-11-2018


Opinion/decision on a Paediatric investigation plan (PIP): Exviera,Dasabuvir (sodium monohydrate), decision type: , therapeutic area: , PIP number: P/0174/2018

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Europe - EMA - European Medicines Agency

22-11-2018


Opinion/decision on a Paediatric investigation plan (PIP): Citric acid (as citric acid anhydrous) / sodium chloride / simeticone / macrogol 4000 / sodium citrate /sodium sulfate (as sodium sulfate anhydrous) / potassium chloride (PMF104), decision type:

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Europe - EMA - European Medicines Agency

19-11-2018


Questions and answers on sodium laurilsulfate used as an excipient in medicinal products for human use

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Questions and answers on sodium laurilsulfate used as an excipient in medicinal products for human use

Europe - EMA - European Medicines Agency

26-9-2018

Kexxtone (Elanco GmbH)

Kexxtone (Elanco GmbH)

Kexxtone (Active substance: Monensin sodium) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)6324 of Wed, 26 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/V/C/2235/T/10

Europe -DG Health and Food Safety

24-9-2018

Inhixa (Techdow Europe AB)

Inhixa (Techdow Europe AB)

Inhixa (Active substance: enoxaparin sodium) - Centralised - Variation - Commission Decision (2018)6101 of Mon, 24 Sep 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4264/X/18, 26

Europe -DG Health and Food Safety

27-8-2018

Arixtra (Aspen Pharma Trading Limited)

Arixtra (Aspen Pharma Trading Limited)

Arixtra (Active substance: Fondaparinux sodium) - PSUSA - Modification - Commission Decision (2018)5708 of Mon, 27 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/403/PSUSA/1467-201712

Europe -DG Health and Food Safety

3-8-2018

Sodium oxybate

Sodium oxybate

Sodium oxybate (Active substance: Sodium oxybate) - Centralised - Art 28 - (PSUR - Commission Decision (2018)5381 of Fri, 03 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/10612/201710

Europe -DG Health and Food Safety

2-8-2018

EU/3/18/2043 (Dr Ulrich Granzer)

EU/3/18/2043 (Dr Ulrich Granzer)

EU/3/18/2043 (Active substance: Combination of carboplatin and sodium valproate) - Orphan designation - Commission Decision (2018)5275 of Thu, 02 Aug 2018 European Medicines Agency (EMA) procedure number: EMA/OD/036/18

Europe -DG Health and Food Safety

11-7-2018

Fosavance (Merck Sharp and Dohme B.V.)

Fosavance (Merck Sharp and Dohme B.V.)

Fosavance (Active substance: Alendronate Sodium / Colecalciferol) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4518 of Wed, 11 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/619/T/42

Europe -DG Health and Food Safety

10-7-2018

Adrovance (Merck Sharp and Dohme B.V.)

Adrovance (Merck Sharp and Dohme B.V.)

Adrovance (Active substance: Alendronate sodium / Colecalciferol) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)4477 of Tue, 10 Jul 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/759/T/39

Europe -DG Health and Food Safety

10-7-2018

Ammonaps (Swedish Orphan Biovitrum International AB)

Ammonaps (Swedish Orphan Biovitrum International AB)

Ammonaps (Active substance: Sodium phenylbutyrate) - Centralised - Yearly update - Commission Decision (2018)4483 of Tue, 10 Jul 2018

Europe -DG Health and Food Safety

5-7-2018

Withdrawn application:  Prohippur, sodium benzoate, Initial authorisation

Withdrawn application: Prohippur, sodium benzoate, Initial authorisation

Europe - EMA - European Medicines Agency

27-6-2018

Yondelis (Pharma Mar S.A.)

Yondelis (Pharma Mar S.A.)

Yondelis (Active substance: Trabectedin) - PSUSA - Modification - Commission Decision (2018)4096 of Wed, 27 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/PSUSA/3001/201709

Europe -DG Health and Food Safety

19-6-2018

Xyrem (UCB Pharma S.A.)

Xyrem (UCB Pharma S.A.)

Xyrem (Active substance: Sodium oxybate) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3912 of Tue, 19 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/593/T/74

Europe -DG Health and Food Safety

1-6-2018

Valproate

Valproate

Valproate (Active substance: medicinal products containing substances related to valproate (sodium valproate, valproic acid, valproate semisodium, valpromide, valproate magnesium)) - Community Referrals - Art 31 - Commission Decision (2018)3623 of Fri, 01 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/A-31/1454

Europe -DG Health and Food Safety

16-5-2018

Busulfan Fresenius Kabi (Fresenius Kabi Deutschland GmbH)

Busulfan Fresenius Kabi (Fresenius Kabi Deutschland GmbH)

Busulfan Fresenius Kabi (Active substance: busulfan) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)3005 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2806/T/8

Europe -DG Health and Food Safety