Country: Ireland
Language: English
Source: HPRA (Health Products Regulatory Authority)
CIMETIDINE
McDermott Laboratories Ltd t/a Gerard Laboratories
800 Milligram
Film Coated Tablet
1991-11-27
License IRISH MEDICINES BOARD ACTS 1995 AND 2006 MEDICINAL PRODUCTS(CONTROL OF PLACING ON THE MARKET)REGULATIONS,2007 (S.I. No.540 of 2007) PA0577/005/003 Case No: 2032354 The Irish Medicines Board in exercise of the powers conferred on it by the above mentioned Regulations hereby grants to McDermott Laboratories Ltd t/a Gerard Laboratories 35/36 Baldoyle Industrial Estate, Grange Road, Dublin 13, Ireland an authorisation, subject to the provisions of the said Regulations, in respect of the product Geramet 800mg Film-coated Tablets 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 28/03/2008. Signed on behalf of the Irish Medicines Board this ________________ A person authorised in that behalf by the said Board. Irish Medicines Board ______________________________________________________________________________________________________________________ Date Printed 25/04/2008 CRN 2032354 page number: 1 Part II Summary of Product Characteristics 1 NAME OF THE MEDICINAL PRODUCT Geramet 800 mg Film-coated Tablets 2 QUALITATIVE AND QUA Read the complete document