Commission Implementing Regulation (EU) 2016/2016 of 17 November 2016 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances acetamiprid, benzoic acid, flazasulfuron, mecoprop-P, mepanipyrim, mesosulfuron, propineb, propoxycarbazon, propyzamide, propiconazole, Pseudomonas chlororaphis Strain: MA 342, pyraclostrobin, quinoxyfen, thiacloprid, thiram, ziram, zoxamide (Text with EEA relevance )

Implementing Regulation (EU) 2016/2016 · Regulation · 3 articles

Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗

Article 1

Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended in accordance with the Annex to this Regulation.

Article 2

This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .

Supplementary provisions

ANNEXSupplementary provisions

ANNEX Part A of the Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: (1) in the sixth column, expiration of approval, of row 54, Propineb, the date is replaced by ‘31 January 2018’; (2) in the sixth column, expiration of approval, of row 55, Propyzamide, the date is replaced by ‘31 January 2018’; (3) in the sixth column, expiration of approval, of row 57, Mecoprop-P, the date is replaced by ‘31 January 2018’; (4) in the sixth column, expiration of approval, of row 58, Propiconazole, the date is replaced by ‘31 January 2018’; (5) in the sixth column, expiration of approval, of row 73, Thiram, the date is replaced by ‘30 April 2018’; (6) in the sixth column, expiration of approval, of row 74, Ziram, the date is replaced by ‘30 April 2018’; (7) in the sixth column, expiration of approval, of row 75, Mesosulfuron, the date is replaced by ‘31 January 2018’; (8) in the sixth column, expiration of approval, of row 76, Propoxycarbazone, the date is replaced by ‘31 January 2018’; (9) in the sixth column, expiration of approval, of row 77, Zoxamide, the date is replaced by ‘31 January 2018’; (10) in the sixth column, expiration of approval, of row 79, Benzoic acid, the date is replaced by ‘31 January 2018’; (11) in the sixth column, expiration of approval, of row 80, Flazasulfuron, the date is replaced by ‘31 January 2018’; (12) in the sixth column, expiration of approval, of row 81, Pyraclostrobin, the date is replaced by ‘31 January 2018’; (13) in the sixth column, expiration of approval, of row 82, Quinoxyfen, the date is replaced by ‘30 April 2018’; (14) in the sixth column, expiration of approval, of row 89, Pseudomonas chlororaphis Strain: MA 342, the date is replaced by ‘30 April 2018’; (15) in the sixth column, expiration of approval, of row 90, Mepanipyrim, the date is replaced by ‘30 April 2018’; (16) in the sixth column, expiration of approval, of row 91, Acetamiprid, the date is replaced by ‘30 April 2018’; (17) in the sixth column, expiration of approval, of row 92, Thiacloprid, the date is replaced by ‘30 April 2018’.

Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

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