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Commission Implementing Regulation (EU) 2022/1480 of 7 September 2022 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 2-phenylphenol (including its salts such as the sodium salt), 8-hydroxyquinoline, amidosulfuron, bensulfuron, bifenox, chlormequat, chlorotoluron, clofentezine, clomazone, daminozide, deltamethrin, dicamba, difenoconazole, diflufenican, dimethachlor, esfenvalerate, etofenprox, fenoxaprop-P, fenpropidin, fenpyrazamine, fludioxonil, flufenacet, flumetralin, fosthiazate, lenacil, MCPA, MCPB, nicosulfuron, paraffin oils, paraffin oil, penconazole, picloram, prohexadione, propaquizafop, prosulfocarb, quizalofop-P-ethyl, quizalofop-P-tefuryl, sodium 5-nitroguaiacolate, sodium o-nitrophenolate, sodium p-nitrophenolate, sulphur, tebufenpyrad, tetraconazole, tri-allate, triflusulfuron and tritosulfuron (Text with EEA relevance)

Commission Implementing Regulation (EU) 2022/1480 of 7 September 2022 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 2-phenylphenol (including its salts such as the sodium salt), 8-hydroxyquinoline, amidosulfuron, bensulfuron, bifenox, chlormequat, chlorotoluron, clofentezine, clomazone, daminozide, deltamethrin, dicamba, difenoconazole, diflufenican, dimethachlor, esfenvalerate, etofenprox, fenoxaprop-P, fenpropidin, fenpyrazamine, fludioxonil, flufenacet, flumetralin, fosthiazate, lenacil, MCPA, MCPB, nicosulfuron, paraffin oils, paraffin oil, penconazole, picloram, prohexadione, propaquizafop, prosulfocarb, quizalofop-P-ethyl, quizalofop-P-tefuryl, sodium 5-nitroguaiacolate, sodium o-nitrophenolate, sodium p-nitrophenolate, sulphur, tebufenpyrad, tetraconazole, tri-allate, triflusulfuron and tritosulfuron (Text with EEA relevance)

Implementing Regulation (EU) 2022/1480 · 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

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 The Annex to Implementing Regulation (EU) No 540/2011 is amended as follows: (a) Part A is amended as follows: (1) in the sixth column, expiration of approval, of row 40, Deltamethrin, the date is replaced by ‘31 October 2023’; (2) in the sixth column, expiration of approval, of row 65, Flufenacet, the date is replaced by ‘31 October 2023’; (3) in the sixth column, expiration of approval, of row 69, Fosthiazate, the date is replaced by ‘31 October 2023’; (4) in the sixth column, expiration of approval, of row 102, Chlorotoluron, the date is replaced by ‘31 October 2023’; (5) in the sixth column, expiration of approval, of row 104, Daminozide, the date is replaced by ‘31 October 2023’; (6) in the sixth column, expiration of approval, of row 107, MCPA, the date is replaced by ‘31 October 2023’; (7) in the sixth column, expiration of approval, of row 108, MCPB, the date is replaced by ‘31 October 2023’; (8) in the sixth column, expiration of approval, of row 160, Prosulfocarb, the date is replaced by ‘31 October 2023’; (9) in the sixth column, expiration of approval, of row 161, Fludioxonil, the date is replaced by ‘31 October 2023’; (10) in the sixth column, expiration of approval, of row 162, Clomazone, the date is replaced by ‘31 October 2023’; (11) in the sixth column, expiration of approval, of row 169, Amidosulfuron, the date is replaced by ‘31 December 2023’; (12) in the sixth column, expiration of approval, of row 170, Nicosulfuron, the date is replaced by ‘31 December 2023’; (13) in the sixth column, expiration of approval, of row 171, Clofentezine, the date is replaced by ‘31 December 2023’; (14) in the sixth column, expiration of approval, of row 172, Dicamba, the date is replaced by ‘31 December 2023’; (15) in the sixth column, expiration of approval, of row 173, Difenoconazole, the date is replaced by ‘31 December 2023’; (16) in the sixth column, expiration of approval, of row 176, Lenacil, the date is replaced by ‘31 December 2023’; (17) in the sixth column, expiration of approval, of row 178, Picloram, the date is replaced by ‘31 December 2023’; (18) in the sixth column, expiration of approval, of row 180, Bifenox, the date is replaced by ‘31 December 2023’; (19) in the sixth column, expiration of approval, of row 181, Diflufenican, the date is replaced by ‘31 December 2023’; (20) in the sixth column, expiration of approval, of row 182, Fenoxaprop-P, the date is replaced by ‘31 December 2023’; (21) in the sixth column, expiration of approval, of row 183, Fenpropidin, the date is replaced by ‘31 December 2023’; (22) in the sixth column, expiration of approval, of row 186, Tritosulfuron, the date is replaced by ‘30 November 2023’; (23) in the sixth column, expiration of approval, of row 271, Bensulfuron, the date is replaced by ‘31 October 2023’; (24) in the sixth column, expiration of approval, of row 272, Sodium 5-nitroguaiacolate, the date is replaced by ‘31 October 2023’; (25) in the sixth column, expiration of approval, of row 273, Sodium o-nitrophenolate, the date is replaced by ‘31 October 2023’; (26) in the sixth column, expiration of approval, of row 274, Sodium p-nitrophenolate, the date is replaced by ‘31 October 2023’; (27) in the sixth column, expiration of approval, of row 275, Tebufenpyrad, the date is replaced by ‘31 October 2023’; (28) in the sixth column, expiration of approval, of row 276, Chlormequat, the date is replaced by ‘30 November 2023’; (29) in the sixth column, expiration of approval, of row 278, Propaquizafop, the date is replaced by ‘30 November 2023’; (30) in the sixth column, expiration of approval, of row 279, Quizalofop-P-ethyl and Quizalofop-P-tefuryl, the date is replaced by ‘30 November 2023’; (31) in the sixth column, expiration of approval, of row 284, Dimethachlor, the date is replaced by ‘31 December 2023’; (32) in the sixth column, expiration of approval, of row 285, Etofenprox, the date is replaced by ‘31 December 2023’; (33) in the sixth column, expiration of approval, of row 287, Penconazole, the date is replaced by ‘31 December 2023’; (34) in the sixth column, expiration of approval, of row 288, Tri-allate, the date is replaced by ‘31 December 2023’; (35) in the sixth column, expiration of approval, of row 289, Triflusulfuron, the date is replaced by ‘31 December 2023’; (36) in the sixth column, expiration of approval, of row 292, Sulphur, the date is replaced by ‘31 December 2023’; (37) in the sixth column, expiration of approval, of row 293, Tetraconazole, the date is replaced by ‘31 December 2023’; (38) in the sixth column, expiration of approval, of row 294, Paraffin oils, the date is replaced by ‘31 December 2023’; (39) in the sixth column, expiration of approval, of row 295, Paraffin oil, the date is replaced by ‘31 December 2023’; (40) in the sixth column, expiration of approval, of row 299, 2-phenylphenol (including its salts such as the sodium salt), the date is replaced by ‘31 December 2023’; (b) Part B is amended as follows: (1) in the sixth column, expiration of approval, of row 6, Prohexadione, the date is replaced by ‘31 December 2023’; (2) in the sixth column, expiration of approval, of row 18, 8-hydroxyquinoline, the date is replaced by ‘31 December 2023’; (3) in the sixth column, expiration of approval, of row 25, Fenpyrazamine, the date is replaced by ‘31 December 2023’; (c) Part E is amended as follows: (1) in the sixth column, expiration of approval, of row 1, Flumetralin, the date is replaced by ‘11 December 2023’; (2) in the sixth column, expiration of approval, of row 2, Esfenvalerate, the date is replaced by ‘31 December 2023’.

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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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