34As the Advocate General noted, in essence, in point 30 of his Opinion, in the light of the definition of the scope of ‘product’, as is clear from the Court’s settled case-law, a literal interpretation of Article 3(d) of Regulation No 469/2009 presupposes that the first MA for the product as a medicinal product within the meaning of that provision means the first MA for a medicinal product incorporating the active ingredient or the combination of active ingredients at issue.
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