Commission Implementing Regulation (EU) 2018/1262 of 20 September 2018 amending Implementing Regulation (EU) No 540/2011 as regards the extension of the approval periods of the active substances 1-methylcyclopropene, beta-cyfluthrin, chlorothalonil, chlorotoluron, clomazone, cypermethrin, daminozide, deltamethrin, dimethenamid-p, diuron, fludioxonil, flufenacet, flurtamone, fosthiazate, indoxacarb, MCPA, MCPB, prosulfocarb, thiophanate-methyl and tribenuron (Text with EEA relevance.)

Implementing Regulation (EU) 2018/1262 · 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

Part A of 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 third day following that of its publication in the Official Journal of the European Union .

Supplementary provisions

ANNEXSupplementary provisions

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 40, Deltamethrin, the date is replaced by ‘31 October 2019’; (2) in the sixth column, expiration of approval, of row 48, Beta-cyfluthrin, the date is replaced by ‘31 October 2019’; (3) in the sixth column, expiration of approval, of row 64, Flurtamone, the date is replaced by ‘31 October 2019’; (4) in the sixth column, expiration of approval, of row 65, Flufenacet, the date is replaced by ‘31 October 2019’; (5) in the sixth column, expiration of approval, of row 67, Dimethenamid-p, the date is replaced by ‘31 October 2019’; (6) in the sixth column, expiration of approval, of row 69, Fosthiazate, the date is replaced by ‘31 October 2019’; (7) in the sixth column, expiration of approval, of row 101, Chlorothalonil, the date is replaced by ‘31 October 2019’; (8) in the sixth column, expiration of approval, of row 102, Chlorotoluron, the date is replaced by ‘31 October 2019’; (9) in the sixth column, expiration of approval, of row 103, Cypermethrin, the date is replaced by ‘31 October 2019’; (10) in the sixth column, expiration of approval, of row 104, Daminozide, the date is replaced by ‘31 October 2019’; (11) in the sixth column, expiration of approval, of row 105, Thiophanate-methyl, the date is replaced by ‘31 October 2019’; (12) in the sixth column, expiration of approval, of row 106, Tribenuron, the date is replaced by ‘31 October 2019’; (13) in the sixth column, expiration of approval, of row 107, MCPA, the date is replaced by ‘31 October 2019’; (14) in the sixth column, expiration of approval, of row 108, MCPB, the date is replaced by ‘31 October 2019’; (15) in the sixth column, expiration of approval, of row 117, 1-methylcyclopropene, the date is replaced by ‘31 October 2019’; (16) in the sixth column, expiration of approval, of row 119, Indoxacarb, the date is replaced by ‘31 October 2019’; (17) in the sixth column, expiration of approval, of row 160, Prosulfocarb, the date is replaced by ‘31 October 2019’; (18) in the sixth column, expiration of approval, of row 161, Fludioxonil, the date is replaced by ‘31 October 2019’; (19) in the sixth column, expiration of approval, of row 162, Clomazone, the date is replaced by ‘31 October 2019’; (20) in the sixth column, expiration of approval, of row 192, Diuron, the date is replaced by ‘30 September 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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