Insol Dermatophyton Zawiesina do wstrzykiwań
Insol Dermatophyton Zawiesina do wstrzykiwań
Authorised
- Trichophyton verrucosum, strain 410, Inactivated
- Trichophyton sarkisovii, strain 551, Inactivated
- Trichophyton equinum, strain 381, Inactivated
- Trichophyton mentagrophytes, strain 1032, Inactivated
- Microsporum canis, strain 1393, Inactivated
- Microsporum distortum, strain 120, Inactivated
- Microsporum obesum, strain 1311, Inactivated
- Microsporum gypseum, strain 59, Inactivated
Product identification
Medicine name:
Insol Dermatophyton Zawiesina do wstrzykiwań
Active substance:
- Trichophyton verrucosum, strain 410, Inactivated
- Trichophyton sarkisovii, strain 551, Inactivated
- Trichophyton equinum, strain 381, Inactivated
- Trichophyton mentagrophytes, strain 1032, Inactivated
- Microsporum canis, strain 1393, Inactivated
- Microsporum distortum, strain 120, Inactivated
- Microsporum obesum, strain 1311, Inactivated
- Microsporum gypseum, strain 59, Inactivated
Target species:
-
Cat
-
Horse
-
Dog
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Trichophyton verrucosum, strain 410, Inactivated
-
Trichophyton sarkisovii, strain 551, Inactivated
-
Trichophyton equinum, strain 381, Inactivated
-
Trichophyton mentagrophytes, strain 1032, Inactivated
-
Microsporum canis, strain 1393, Inactivated
-
Microsporum distortum, strain 120, Inactivated
-
Microsporum obesum, strain 1311, Inactivated
-
Microsporum gypseum, strain 59, Inactivated
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cat
-
All relevant tissuesno withdrawal periodThe withdrawal period does not apply.
-
- Horse
- Dog
-
All relevant tissuesno withdrawal periodThe withdrawal period does not apply.
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI05AQ02
- QI06AQ01
- QI07AQ01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
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:
- Boehringer Ingelheim Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Wirtschaftsgenossenschaft Deutscher Tierarzte eG
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 1405
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Labelling
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 27/04/2022
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: 27/04/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 6/02/2023
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