Folltropin 700 IU Powder and Solvent for solution for injection
Folltropin 700 IU Powder and Solvent for solution for injection
Authorised
- Follicle stimulating hormone, porcine
Product identification
Medicine name:
Folltropin 700 IU Powder and Solvent for solution for injection
Folltropin 700 j.m./ fiolkę Proszek i rozpuszczalnik do sporządzania roztworu do wstrzykiwań
Active substance:
- Follicle stimulating hormone, porcine
Target species:
-
Cattle
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Follicle stimulating hormone, porcine700.00/international unit(s)1.00Vial
Pharmaceutical form:
-
Powder and solvent for solution for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG03GA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- Cardboard box containing one vial of powder and one vial of solvent.Freeze-dried powderClear glass 20 ml vial (Type I), with halobutyl rubber stopper (Type I) and red flip-off cap.SolventClear glass 20 ml vial (Type I), with halobutyl rubber stopper (Type I) and yellow flip-off cap.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Vetoquinol Biowet Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetoquinol S.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2348
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0126/001
Concerned member states:
-
Austria
-
Czechia
-
Denmark
-
France
-
Germany
-
Italy
-
Netherlands
-
Poland
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 18/11/2025
Package Leaflet
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in another language below.
Polish (PDF)
Published on: 18/11/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 18/11/2025