Country: Ireland
Language: English
Source: HPRA (Health Products Regulatory Authority)
AMOXICILLIN TRIHYDRATE
Generics (UK) Limited
125 MG/5ml
Powder for Oral Suspension
1989-11-20
License IRISH MEDICINES BOARD ACTS 1995 AND 2006 MEDICINAL PRODUCTS(CONTROL OF PLACING ON THE MARKET)REGULATIONS,2007 (S.I. No.540 of 2007) PA0405/005/003 Case No: 2043367 The Irish Medicines Board in exercise of the powers conferred on it by the above mentioned Regulations hereby grants to Generics (UK) Limited 12 Station Close, Potters Bar, Hertfordshire EN6 1TL, United Kingdom an authorisation, subject to the provisions of the said Regulations, in respect of the product Geramox 125mg/5 ml Powder for Oral Suspension. The particulars of which are set out in Part I and Part II of the attached Schedule. The authorisation is also subject to the general conditions as may be specified in the said Regulations as listed on the reverse of this document. This authorisation, unless previously revoked, shall continue in force from 30/04/2008. Signed on behalf of the Irish Medicines Board this ________________ A person authorised in that behalf by the said Board. Irish Medicines Board ______________________________________________________________________________________________________________________ Date Printed 26/05/2010 CRN 2043367 page number: 1 Part II Summary of Product Characteristics 1 NAME OF THE MEDICINAL PRODUCT Geramox 125mg/5ml Powder for Oral Suspension 2 QUALITATIVE AND& Read the complete document