Land: Irland
Sprog: engelsk
Kilde: HPRA (Health Products Regulatory Authority)
CEFTIOFUR
Pfizer Healthcare Ireland
QJ01DD90
1.06 Grams
Pdr for Soln for Injection
Antibacterial
Bovine
2006-05-19
IRISH MEDICINES BOARD ACT 1995, AS AMENDED EUROPEAN COMMUNITIES (ANIMAL REMEDIES) (NO. 2) REGULATIONS 2007 VPA: 10019/086/001 Case No: 7005553 The Irish Medicines Board in exercise of the powers conferred on it by Animal Remedies (No. 2) Regulations (S.I. No. 786 of 2007) hereby grants to: PFIZER HEALTHCARE IRELAND TRADING AS: PFIZER ANIMAL HEALTH, RINGASKIDDY, CO. CORK, IRELAND an authorisation, subject to the provisions of the said Regulations and the general conditions of the attached authorisation, in respect of the Veterinary Medicinal Product: EXCENEL 1 G STERILE POWDER FOR SOLUTION FOR INJECTION The particulars of which are set out in the attached Schedule. The authorisation is also subject to any special conditions as may be specified in the Schedule. The authorisation,unless revoked, shall continue in force from 09/08/2010. Signed on behalf of the Irish Medicines Board ________________ A person authorised in that behalf by the said Board. (NOTE: This authorisation replaces any previous authorisation in respect of this product which is now null and void.) IRISH MEDICINES BOARD ________________________________________________________________________________________________________________________ _Date Printed 10/08/2010_ _CRN 7005553_ _page number: 1_ PART II SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE VETERINARY MEDICINAL PRODUCT Excenel 1 g Sterile Powder for Solution for Injection 2 QUALITATIVE AND QUANTITATIVE COMPOSITION Each vial contains : ACTIVE SUBSTANCE: Ceftiofur 1.06g (as cetiofur sodium) When reconstituted with 20 ml water for injection, each ml of reconstituted solution contains ceftiofur 50mg. For a full list of excipients, see section 6.1 3 PHARMACEUTICAL FORM Powder for solution for injection. A white to light brown freeze dried powder. 4 CLINICAL PARTICULARS 4.1 TARGET SP Læs hele dokumentet