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Commission Implementing Regulation (EU) 2026/372 of 20 February 2026 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-decanol, 1-naphthylacetamide, 1-naphthylacetic acid, 6-benzyladenine, aluminium sulfate, boscalid, dodine, esfenvalerate, eugenol, fenpyroximate, fluazifop-P, fluazinam, fluometuron, fluopyram, flutolanil, geraniol, malathion, penoxsulam, pinoxaden, prohexadione, proquinazid, prosulfuron, pyrethrins, pyridaben, pyrimethanil, sintofen, spiroxamine, sulphur and thymol

Implementing Regulation (EU) 2026/372 · 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 1. 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 135, Pyrimethanil, the date is replaced by ‘30 June 2027’; (2) in the sixth column, expiration of approval, of row 164, Boscalid, the date is replaced by ‘31 March 2028’; (3) in the sixth column, expiration of approval, of row 187, Flutolanil, the date is replaced by ‘15 June 2027’; (4) in the sixth column, expiration of approval, of row 189, Fluazinam, the date is replaced by ‘30 November 2027’; (5) in the sixth column, expiration of approval, of row 213, Fenpyroximate, the date is replaced by ‘31 January 2028’; (6) in the sixth column, expiration of approval, of row 246, Pyrethrins, the date is replaced by ‘30 April 2028’; (7) in the sixth column, expiration of approval, of row 292, Sulphur, the date is replaced by ‘31 July 2027’; (8) in the sixth column, expiration of approval, of row 300, Malathion, the date is replaced by ‘15 July 2028’; (9) in the sixth column, expiration of approval, of row 301, Penoxsulam, the date is replaced by ‘15 May 2027’; (10) in the sixth column, expiration of approval, of row 302, Proquinazid, the date is replaced by ‘31 December 2027’; (11) in the sixth column, expiration of approval, of row 313, Pyridaben, the date is replaced by ‘31 January 2030’; (12) in the sixth column, expiration of approval, of row 317, 6-benzyladenine, the date is replaced by ‘15 January 2030’; (13) in the sixth column, expiration of approval, of row 323, Dodine, the date is replaced by ‘30 June 2028’; (14) in the sixth column, expiration of approval, of row 333, 1-decanol, the date is replaced by ‘30 June 2028’; (15) in the sixth column, expiration of approval, of row 335, Fluometuron, the date is replaced by ‘15 January 2030’; (16) in the sixth column, expiration of approval, of row 341, Sintofen, the date is replaced by ‘15 January 2030’; (17) in the sixth column, expiration of approval, of row 346, Aluminium sulfate, the date is replaced by ‘15 January 2030’. 2. Part B of the Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: (1) in the sixth column, expiration of approval, of row 6, Prohexadione, the date is replaced by ‘15 May 2028’; (2) in the sixth column, expiration of approval, of row 7, Spiroxamine, the date is replaced by ‘30 November 2029’; (3) in the sixth column, expiration of approval, of row 12, 1-naphthylacetamide, the date is replaced by ‘30 November 2029’; (4) in the sixth column, expiration of approval, of row 13, 1-naphthylacetic acid, the date is replaced by ‘30 November 2029’; (5) in the sixth column, expiration of approval, of row 15, Fluazifop-P, the date is replaced by ‘30 November 2029’; (6) in the sixth column, expiration of approval, of row 45, Eugenol, the date is replaced by ‘15 April 2028’; (7) in the sixth column, expiration of approval, of row 46, Geraniol, the date is replaced by ‘15 April 2028’; (8) in the sixth column, expiration of approval, of row 47, Thymol, the date is replaced by ‘15 April 2028’; (9) in the sixth column, expiration of approval, of row 51, Fluopyram, the date is replaced by ‘15 June 2028’; (10) in the sixth column, expiration of approval, of row 97, Pinoxaden, the date is replaced by ‘31 December 2029’. 3. Part E of the Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: (1) in the sixth column, expiration of approval, of row 2, Esfenvalerate, the date is replaced by ‘30 November 2029’; (2) in the sixth column, expiration of approval, of row 6, Prosulfuron, the date is replaced by ‘15 December 2029’.

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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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