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Commission Implementing Regulation (EU) 2023/1757 of 11 September 2023 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances bensulfuron, chlormequat, chlorotoluron, clomazone, daminozide, deltamethrin, eugenol, fludioxonil, flufenacet, flumetralin, fosthiazate, geraniol, MCPA, MCPB, propaquizafop, prosulfocarb, quizalofop-P-ethyl, quizalofop-P-tefuryl, sodium 5-nitroguaiacolate, sodium o-nitrophenolate, sodium p-nitrophenolate, sulfuryl fluoride, tebufenpyrad, thymol, and tritosulfuron (Text with EEA relevance)

Implementing Regulation (EU) 2023/1757 · 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 twentieth day following that of its publication in the Official Journal of the European Union .

Supplementary provisions

ANNEXSupplementary provisions

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ANNEX The Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: 1. Part A is amended as follows: (1) in the sixth column, expiration of approval, of row 40, Deltamethrin, the date is replaced by ‘15 August 2026’; (2) in the sixth column, expiration of approval, of row 65, Flufenacet, the date is replaced by ‘15 June 2025’; (3) in the sixth column, expiration of approval, of row 69, Fosthiazate, the date is replaced by ‘31 January 2027’; (4) in the sixth column, expiration of approval, of row 102, Chlorotoluron, the date is replaced by ‘15 August 2026’; (5) in the sixth column, expiration of approval, of row 104, Daminozide, the date is replaced by ‘15 September 2025’; (6) in the sixth column, expiration of approval, of row 107, MCPA, the date is replaced by ‘15 August 2026’; (7) in the sixth column, expiration of approval, of row 108, MCPB, the date is replaced by ‘15 August 2026’; (8) in the sixth column, expiration of approval, of row 160, Prosulfocarb, the date is replaced by ‘31 January 2027’; (9) in the sixth column, expiration of approval, of row 161, Fludioxonil, the date is replaced by ‘15 June 2025’; (10) in the sixth column, expiration of approval, of row 162, Clomazone, the date is replaced by ‘15 June 2025’; (11) in the sixth column, expiration of approval, of row 186, Tritosulfuron, the date is replaced by ‘15 July 2025’; (12) in the sixth column, expiration of approval, of row 271, Bensulfuron, the date is replaced by ‘15 August 2026’; (13) in the sixth column, expiration of approval, of row 272, Sodium 5-nitroguaiacolate, the date is replaced by ‘31 January 2027’; (14) in the sixth column, expiration of approval, of row 273, Sodium o-nitrophenolate, the date is replaced by ‘31 January 2027’; (15) in the sixth column, expiration of approval, of row 274, Sodium p-nitrophenolate, the date is replaced by ‘31 January 2027’; (16) in the sixth column, expiration of approval, of row 275, Tebufenpyrad, the date is replaced by ‘31 January 2027’; (17) in the sixth column, expiration of approval, of row 276, Chlormequat, the date is replaced by ‘28 February 2027’; (18) in the sixth column, expiration of approval, of row 278, Propaquizafop, the date is replaced by ‘28 February 2027’; (19) in the sixth column, expiration of approval, of row 279, Quizalofop-P-ethyl and Quizalofop-P-tefuryl, the date is replaced by ‘28 February 2027’; (20) in the sixth column, expiration of approval, of row 307, Sulfuryl fluoride, the date is replaced by ‘31 January 2027’. 2. Part B is amended as follows: (1) in the sixth column, expiration of approval, of row 45, Eugenol, the date is replaced by ‘30 April 2026’; (2) in the sixth column, expiration of approval, of row 46, Geraniol, the date is replaced by ‘30 April 2026’; (3) in the sixth column, expiration of approval, of row 47, Thymol, the date is replaced by ‘30 April 2026’; 3. Part E is amended as follows: in the sixth column, expiration of approval, of row 1, Flumetralin, the date is replaced by ‘ 11 May 2026 ’.

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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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