Review Product Marketing Authorisation For Human Use "histamine Hal Allergy»

Original Language Title: Modifica dell'autorizzazione all'immissione in commercio delmedicinale per uso umano «Istamina Hal Allergy»

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Retrieved November 20, 2014 at the # 2426/2014 V & determines are authorized the following variation: introduction of the Risk Management Plan, in relation to the medicinal product authorised packaging HAL ALLERGY and HISTAMINE the placing in Italy following the mutual recognition procedure.
How to: NL/H/2307/001/II/002.
Types of variation: c. 1. z) other variation.
A.I.C. Holder: Hal Allergy B.V.
Inventory disposal lots already products can be kept on the market until the expiration date printed on the label of the medicinal product in accordance with art. 1, paragraph 5 of the April 14, 2014 # 371 determines AIFA published in Official Gazette No 101 of May 3, 2014.
Date of determination: this determination is effective on the day following that of its publication, to decompress, in Gazzetta Ufficiale della Repubblica italiana and company will be notified to the holder of the marketing authorisation for the medicinal product.