Country: Ireland
Language: English
Source: HPRA (Health Products Regulatory Authority)
ESCITALOPRAM
Pliva Pharma Limited
5 Milligram
Film Coated Tablet
2009-05-28
License IRISH MEDICINES BOARD ACTS 1995 AND 2006 MEDICINAL PRODUCTS(CONTROL OF PLACING ON THE MARKET)REGULATIONS,2007 (S.I. No.540 of 2007) PA0585/037/001 Case No: 2044816 The Irish Medicines Board in exercise of the powers conferred on it by the above mentioned Regulations hereby grants to Pliva Pharma Limited Vision House, Bedford Road, Petersfield, Hampshire GU32 3QB, United Kingdom an authorisation, subject to the provisions of the said Regulations, in respect of the product Escitalopram 5mg 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 28/05/2009 until 27/05/2014. Signed on behalf of the Irish Medicines Board this ________________ A person authorised in that behalf by the said Board. Irish Medicines Board ______________________________________________________________________________________________________________________ Date Printed 29/05/2009 CRN 2044816 page number: 1 Part II Summary of Product Characteristics 1 NAME OF THE MEDICINAL PRODUCT Escitalopram 5mg Film-coated Tablets 2 QUALITATIVE AND QUANT Read the complete document