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Commission Implementing Regulation (EU) 2018/1796 of 20 November 2018 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances amidosulfuron, bifenox, chlorpyrifos, chlorpyrifos-methyl, clofentezine, dicamba, difenoconazole, diflubenzuron, diflufenican, dimoxystrobin, fenoxaprop-p, fenpropidin, lenacil, mancozeb, mecoprop-p, metiram, nicosulfuron, oxamyl, picloram, pyraclostrobin, pyriproxyfen and tritosulfuron (Text with EEA relevance.)

Implementing Regulation (EU) 2018/1796 · 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

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

Article 2

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

Supplementary provisions

ANNEXSupplementary provisions

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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 57, Mecoprop-P, the date is replaced by ‘31 January 2020’; (2) in the sixth column, expiration of approval, of row 81, Pyraclostrobin, the date is replaced by ‘31 January 2020’; (3) in the sixth column, expiration of approval, of row 111, Chlorpyrifos, the date is replaced by ‘31 January 2020’; (4) in the sixth column, expiration of approval, of row 112, Chlorpyrifos-methyl, the date is replaced by ‘31 January 2020’; (5) in the sixth column, expiration of approval, of row 114, Mancozeb, the date is replaced by ‘31 January 2020’; (6) in the sixth column, expiration of approval, of row 115, Metiram, the date is replaced by ‘31 January 2020’; (7) in the sixth column, expiration of approval, of row 116, Oxamyl, the date is replaced by ‘31 January 2020’; (8) in the sixth column, expiration of approval, of row 128, Dimoxystrobin, the date is replaced by ‘31 January 2020’; (9) in the sixth column, expiration of approval, of row 169, Amidosulfuron, the date is replaced by ‘31 December 2019’; (10) in the sixth column, expiration of approval, of row 170, Nicosulfuron, the date is replaced by ‘31 December 2019’; (11) in the sixth column, expiration of approval, of row 171, Clofentezine, the date is replaced by ‘31 December 2019’; (12) in the sixth column, expiration of approval, of row 172, Dicamba, the date is replaced by ‘31 December 2019’; (13) in the sixth column, expiration of approval, of row 173, Difenoconazole, the date is replaced by ‘31 December 2019’; (14) in the sixth column, expiration of approval, of row 174, Diflubenzuron, the date is replaced by ‘31 December 2019’; (15) in the sixth column, expiration of approval, of row 176, Lenacil, the date is replaced by ‘31 December 2019’; (16) in the sixth column, expiration of approval, of row 178, Picloram, the date is replaced by ‘31 December 2019’; (17) in the sixth column, expiration of approval, of row 179, Pyriproxyfen, the date is replaced by ‘31 December 2019’; (18) in the sixth column, expiration of approval, of row 180, Bifenox, the date is replaced by ‘31 December 2019’; (19) in the sixth column, expiration of approval, of row 181, Diflufenican, the date is replaced by ‘31 December 2019’; (20) in the sixth column, expiration of approval, of row 182, Fenoxaprop-P, the date is replaced by ‘31 December 2019’; (21) in the sixth column, expiration of approval, of row 183, Fenpropidin, the date is replaced by ‘31 December 2019’; (22) in the sixth column, expiration of approval, of row 186, Tritosulfuron, the date is replaced by ‘30 November 2019’.

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

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