Review Of The Marketing Authorisation For Veterinary Agency «Soluzioneiniettabile 250 Μ G/ml Bovine Cyclix» And «Cyclix Μ G/ml Solution For Injection 87.5 Pigs. "

Original Language Title: Modifica dell'autorizzazione all'immissione in commercio deimedicinali per uso veterinario «Cyclix Bovini 250 µg/ml soluzioneiniettabile» e «Cyclix Suini 87,5 µg/ml soluzione iniettabile».

Read the untranslated law here:

Measure # 117 of 250 µ g Cyclix Cattle veterinary medicinal products: February 24, 2015/ml solution for injection 20 ml bottle packaging: A.I.C. # 103,765,018;
bottle of 50 ml A.I.C. # 103,765,020;
Μ g/ml solution for injection Porcine Cyclix 87.5 packaging: bottle of 20 ml A.I.C. # 103,764,015;
bottle of 50 ml A.I.C. # 103,764,027.
A.I.C. holder: Virbac S.A. 1ere Avenue-2065 m L.I.D. 06516 Carros, France.
The object of the measure: change in type a. 7: delete site production and batch release.
Mutual recognition procedure # DE/V/xxxx/IA/014/G.
Is authorized, in respect of veterinary medicinal products given in object, deleting the following site responsible for all stages of production of the finished product, including the batch release: INTERVET International GmbH, Unterschleissheim 85716 Feldstrasse 1A Germany.
Remains entitled to the following site: VIRBAC S.A. 1ere Avenue-2065 m L.I.D. 06516 Carros, France.
Lots already products can remain on the market until the expiration date.
This abstract will be published in the official journal of the Italian Republic, and its decision will be notified to the undertaking in question.