Equimax oral gel for horses
Equimax oral gel for horses
Authorised
- Ivermectin
- Praziquantel
Product identification
Medicine name:
Equimax oral gel for horses
Equimax perorálny gél pre kone
Active substance:
- Ivermectin
- Praziquantel
Target species:
-
Horse
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Ivermectin18.70milligram(s)1.00gram(s)
-
Praziquantel140.30milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral gel
Withdrawal period by route of administration:
-
Oral use
-
Horse
-
Meat and offal35day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP54AA51
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Package description:
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 7.49 grams of product and is fitted with variable dose capacity.Product presentations:Box of 48 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 7.49 grams of product and is fitted with variable dose capacity.Product presentations:Box of 40 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 7.49 grams of product and is fitted with variable dose capacity.Product presentations:Box of 12 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 7.49 grams of product and is fitted with variable dose capacity.Product presentations:Box of 2 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 7.49 grams of product and is fitted with variable dose capacity.Product presentations:Box of 1 syringe or Blister of one syringe.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 6.42 grams of product and is fitted with variable dose capacity.Product presentations:Box of 48 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 6.42 grams of product and is fitted with variable dose capacity.Product presentations:Box of 40 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 6.42 grams of product and is fitted with variable dose capacity.Product presentations:Box of 12 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 6.42 grams of product and is fitted with variable dose capacity.Product presentations:Box of 2 syringes.
- An adjustable multidose syringe consisting of high density polyethylene (white) and low density polyethylene (white).The syringe contains 6.42 grams of product and is fitted with variable dose capacity.Product presentations:Box of 1 syringe or Blister of one syringe.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Sofarimex-Industria Quimica E Farmaceutica S.A.
- Virbac
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/055/MR/05-S
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0501/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
This document does not exist in this language (English). You can find it
in another language below.
Slovak (PDF)
Published on: 9/04/2024
Summary of Product Characteristics
English (PDF)
Download Published on: 3/05/2024
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