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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 1-20 of 169 matching medicines

Product listings were last updated on 01/02/2023
Trade Name Licence Number & Holder Documents
Panacur 10 % w/v Oral Suspension
Oral suspension

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VPA10996/111/001
Authorised: 01/10/1999
Intervet Ireland Limited
SPC Variations
Panacur Equine Granules 22.2 % w/w
Granules

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VPA10996/113/001
Authorised: 01/10/1999
Intervet Ireland Limited
SPC Variations
Panacur Equine Oral Paste 18.75 %w/w
Oral paste

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VPA10996/118/001
Authorised: 01/10/1999
Intervet Ireland Limited
SPC Variations
Panacur PetPaste 187.5 mg/g oral paste for dogs and cats
Oral paste

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VPA10996/188/001
Authorised: 23/09/2005
Intervet Ireland Limited
SPC Variations
Panomec 10 mg/ml Solution for Injection for Cattle, Sheep and Pigs
Solution for injection

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VPA10454/073/001
Authorised: 19/12/1995
Boehringer Ingelheim Vetmedica GmbH
SPC Variations
Paracox-5, suspension for oral suspension for chickens
Suspension for oral suspension

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VPA10996/215/001
Authorised: 23/07/2010
Intervet Ireland Limited
SPC Variations
Paracox-8, suspension for oral suspension for chickens
Suspension for oral suspension

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VPA10996/245/001
Authorised: 19/10/2007
Intervet Ireland Limited
SPC Variations
Parafend 2.265 % Oral Suspension
Oral suspension

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VPA22664/040/001
Authorised: 10/02/1994
Norbrook Laboratories (Ireland) Limited
SPC
Parafend Plus Oral Suspension
Oral suspension

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VPA22664/070/001
Authorised: 30/06/2003
Norbrook Laboratories (Ireland) Limited
SPC
Paramectin 0.08% w/v Drench for Sheep
Oral suspension

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VPA22664/061/001
Authorised: 12/01/2001
Norbrook Laboratories (Ireland) Limited
SPC IPAR Variations
Paramectin 0.5 % Pour-On Solution for Cattle
Pour-on solution

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VPA22664/066/001
Authorised: 29/06/2001
Norbrook Laboratories (Ireland) Limited
SPC Variations
Paramectin 1% Solution for Injection
Solution for injection

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VPA22664/065/001
Authorised: 29/06/2001
Norbrook Laboratories (Ireland) Limited
SPC IPAR Variations
Paramove, 49.5% w/w Hydrogen Peroxide concentrate for solution for fish treatment
Concentrate for solution for fish treatment

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VPA10480/001/001
Authorised: 11/01/2013
Solvay Chemicals International S.A
SPC
Parazole 10% w/v Oral Suspension
Oral suspension

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VPA10484/021/001
Authorised: 01/10/1997
Foran Healthcare Limited
SPC IPAR Variations
Parazole Dog/Cat 100 mg/ml Oral Suspension
Oral suspension

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VPA10484/022/001
Authorised: 21/09/2018
Foran Healthcare Limited
SPC IPAR Variations
Parex 134 mg spot-on solution for medium dogs
Spot-on solution

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VPA10515/002/002
Authorised: 25/11/2013
CF Pharma Limited
SPC
Parex 268 mg spot-on solution for large dogs
Spot-on solution

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VPA10515/002/003
Authorised: 25/11/2013
CF Pharma Limited
SPC
Parex 402 mg spot-on solution for very large dogs
Spot-on solution

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VPA10515/002/004
Authorised: 25/11/2013
CF Pharma Limited
SPC
Parex 50 mg spot-on solution for cats
Spot-on solution

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VPA10515/001/001
Authorised: 25/11/2013
CF Pharma Limited
SPC
Parex 67 mg spot-on solution for small dogs
Spot-on solution

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VPA10515/002/001
Authorised: 25/11/2013
CF Pharma Limited
SPC