Source

Commission Implementing Regulation (EU) 2021/1449 of 3 September 2021 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, bifenox, chlormequat, chlorotoluron, clofentezine, clomazone, cypermethrin, daminozide, deltamethrin, dicamba, difenoconazole, diflufenican, dimethachlor, etofenprox, fenoxaprop-P, fenpropidin, fludioxonil, flufenacet, fosthiazate, indoxacarb, lenacil, MCPA, MCPB, nicosulfuron, paraffin oils, paraffin oil, penconazole, picloram, propaquizafop, prosulfocarb, quizalofop-P-ethyl, quizalofop-P-tefuryl, sulphur, tetraconazole, tri-allate, triflusulfuron and tritosulfuron (Text with EEA relevance)

Implementing Regulation (EU) 2021/1449 · 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 18, 8-hydroxyquinoline, the date is replaced by ‘31 December 2022’; (2) in the sixth column, expiration of approval, of row 40, Deltamethrin, the date is replaced by ‘31 October 2022’; (3) in the sixth column, expiration of approval, of row 65, Flufenacet, the date is replaced by ‘31 October 2022’; (4) in the sixth column, expiration of approval, of row 69, Fosthiazate, the date is replaced by ‘31 October 2022’; (5) in the sixth column, expiration of approval, of row 102, Chlorotoluron, the date is replaced by ‘31 October 2022’; (6) in the sixth column, expiration of approval, of row 103, Cypermethrin, the date is replaced by ‘31 October 2022’; (7) in the sixth column, expiration of approval, of row 104, Daminozide, the date is replaced by ‘31 October 2022’; (8) in the sixth column, expiration of approval, of row 107, MCPA, the date is replaced by ‘31 October 2022’; (9) in the sixth column, expiration of approval, of row 108, MCPB, the date is replaced by ‘31 October 2022’; (10) in the sixth column, expiration of approval, of row 119, Indoxacarb, the date is replaced by ‘31 October 2022’; (11) in the sixth column, expiration of approval, of row 160, Prosulfocarb, the date is replaced by ‘31 October 2022’; (12) in the sixth column, expiration of approval, of row 161, Fludioxonil, the date is replaced by ‘31 October 2022’; (13) in the sixth column, expiration of approval, of row 162, Clomazone, the date is replaced by ‘31 October 2022’; (14) in the sixth column, expiration of approval, of row 169, Amidosulfuron, the date is replaced by ‘31 December 2022’; (15) in the sixth column, expiration of approval, of row 170, Nicosulfuron, the date is replaced by ‘31 December 2022’; (16) in the sixth column, expiration of approval, of row 171, Clofentezine, the date is replaced by ‘31 December 2022’; (17) in the sixth column, expiration of approval, of row 172, Dicamba, the date is replaced by ‘31 December 2022’; (18) in the sixth column, expiration of approval, of row 173, Difenoconazole, the date is replaced by ‘31 December 2022’; (19) in the sixth column, expiration of approval, of row 176, Lenacil, the date is replaced by ‘31 December 2022’; (20) in the sixth column, expiration of approval, of row 178, Picloram, the date is replaced by ‘31 December 2022’; (21) in the sixth column, expiration of approval, of row 180, Bifenox, the date is replaced by ‘31 December 2022’; (22) in the sixth column, expiration of approval, of row 181, Diflufenican, the date is replaced by ‘31 December 2022’; (23) in the sixth column, expiration of approval, of row 182, Fenoxaprop-P, the date is replaced by ‘31 December 2022’; (24) in the sixth column, expiration of approval, of row 183, Fenpropidin, the date is replaced by ‘31 December 2022’; (25) in the sixth column, expiration of approval, of row 186, Tritosulfuron, the date is replaced by ‘30 November 2022’; (26) in the sixth column, expiration of approval, of row 276, Chlormequat, the date is replaced by ‘30 November 2022’; (27) in the sixth column, expiration of approval, of row 278, Propaquizafop, the date is replaced by ‘30 November 2022’; (28) in the sixth column, expiration of approval, of row 279, Quizalofop-P-ethyl and Quizalofop-P-tefuryl, the date is replaced by ‘30 November 2022’; (29) in the sixth column, expiration of approval, of row 284, Dimethachlor, the date is replaced by ‘31 December 2022’; (30) in the sixth column, expiration of approval, of row 285, Etofenprox, the date is replaced by ‘31 December 2022’; (31) in the sixth column, expiration of approval, of row 287, Penconazole, the date is replaced by ‘31 December 2022’; (32) in the sixth column, expiration of approval, of row 288, Tri-allate, the date is replaced by ‘31 December 2022’; (33) in the sixth column, expiration of approval, of row 289, Triflusulfuron, the date is replaced by ‘31 December 2022’; (34) in the sixth column, expiration of approval, of row 292, Sulphur, the date is replaced by ‘31 December 2022’; (35) in the sixth column, expiration of approval, of row 293, Tetraconazole, the date is replaced by ‘31 December 2022’; (36) in the sixth column, expiration of approval, of row 294, Paraffin oils, the date is replaced by ‘31 December 2022’; (37) in the sixth column, expiration of approval, of row 295, Paraffin oil, the date is replaced by ‘31 December 2022’; (38) 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 2022’.

Other acts of the same type

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

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