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For Summary of Product Characteristics (SPCs) of new products that have been granted a marketing authorisation since February 2022 in accordance with Regulation 2019/6, the format and content of the SPC has changed compared to those issued beforehand. In particular sections 7, 8, 9 and 10 (specifying information on the marketing authorisation holder, marketing authorisation number, date of first authorisation and date of revision of the text) are not included in the SPC document itself (these fields appear blank), as this information is provided on the national-specific product information landing page of the website (from which you click through to the SPC document itself).

The HPRA advises healthcare professionals not to retain printed versions of SPC documents, as these documents are subject to change and updating, including changes to safety and dose related information. We recommend that you visit our website as necessary to access the most up-to-date versions. If you have any queries about the SPCs on our website e-mail vetinfo@hpra.ie


  • Veterinary Medicines
 
 

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Latest list of Authorised or Transfer Pending Products
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Showing 1-14 of 14 matching medicines

Product listings were last updated on 29/11/2022
Trade Name Licence Number & Holder Documents
CTC 10 %w/w Oral Powder
Oral powder

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VPA10990/018/001
Authorised: 01/10/1988
Univet Limited
SPC
CTC 10 %w/w Premix for Medicated Feed
Premix for medicated feeding stuff

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VPA10990/039/001
Authorised: 23/06/2006
Univet Limited
SPC
CTC 15 %w/w Premix for Medicated Feed
Premix for medicated feeding stuff

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VPA10990/039/002
Authorised: 23/06/2006
Univet Limited
SPC
CTC 15% w/w Oral Powder
Oral powder

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VPA10990/034/001
Authorised: 19/02/1999
Univet Limited
SPC
Curacef duo, 50 mg/ml / 150 mg/ml, Suspension for Injection for Cattle
Suspension for injection

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VPA10988/092/001
Authorised: 01/08/2014
Virbac S.A.
SPC
Curafluke 10% w/v Oral Drench
Oral suspension

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VPA10990/032/002
Authorised: 15/09/2000
Univet Limited
SPC Variations
Curafluke 5% w/v Oral Drench
Oral suspension

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VPA10990/032/001
Authorised: 05/09/1997
Univet Limited
SPC Variations
Curazole 10 %w/v Oral Drench
Oral suspension

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VPA10990/015/001
Authorised: 07/05/1991
Univet Limited
SPC Variations
Curazole 2.5% w/v Oral Drench
Oral suspension

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VPA10990/015/002
Authorised: 14/05/1992
Univet Limited
SPC Variations
Curazole 5 %w/v Oral Drench
Oral suspension

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VPA10990/015/003
Authorised: 12/03/1992
Univet Limited
SPC Variations
Curazole 5% w/w Premix for Medicated Feed
Premix for medicated feeding stuff

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VPA10990/030/001
Authorised: 26/06/1998
Univet Limited
SPC IPAR
Curazole 50 mg/g oral powder for pigs
Oral powder

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VPA10990/044/001
Authorised: 29/07/2011
Univet Limited
SPC
Curofen 50 mg/g oral powder for pigs
Oral powder

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VPA10990/045/001
Authorised: 06/11/2015
Univet Limited
SPC IPAR
Curofen 50 mg/g Premix for Medicated Feeding Stuff for Pigs
Premix for medicated feeding stuff

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VPA10990/046/001
Authorised: 08/09/2017
Univet Limited
SPC IPAR