# Commission Implementing Regulation (EU) 2015/1013 of 25 June 2015 laying down rules in respect of Regulation (EC) No 273/2004 of the European Parliament and of the Council on drug precursors and of Council Regulation (EC) No 111/2005 laying down rules for the monitoring of trade between the Union and third countries in drug precursors (Text with EEA relevance), Division 3: Box 23: Indicate the authorised maximum quantity and net weight. For Category 4, enter the total net weight of the scheduled substance contained in the consignment of medicinal products.

Extent: E+W+S+N.I.

Column 24: Indicate the quantity available in part 1 and the quantity of the partial export quantity in part 2. For Category 4, enter the total net weight quantity of the scheduled substance contained in the consignment of medicinal products.
Column 25: Indicate the partial export quantity in words.
Box 26: Reference number and the date of the customs declaration.
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Source: https://www.legislation.gov.uk/eur/2015/1013/annex/III/annotations/2/annotation/3 (the official version)
Page: https://openlegislation.uk/eu-regulation-2015-1013/annex-III/annotations/2/annotation/3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.