Agroseller Propyzamid-II

Hauptinformation

  • Handelsname:
  • Agroseller Propyzamid-II
  • Darreichungsform:
  • SC Suspensionskonzentrat
  • Verwenden für:
  • Pflanzen
  • Art der Medizin:
  • Agrochemisch

Dokumenten

  • Information für medizinisches Fachpersonal:
  • Das Informationsblatt für dieses Produkt ist derzeit nicht verfügbar, können Sie eine Anfrage an unseren Kundendienst zu senden und wir werden Sie benachrichtigen, sobald wir in der Lage, um es zu erhalten.


    Fordern Sie die Packungsbeilage für medizinisches Fachpersonal.

Lokalisierung

  • Erhältlich in:
  • Agroseller Propyzamid-II
    Schweiz
  • Sprache:
  • Deutsch

Therapeutische Informationen

  • Therapiegruppe:
  • Herbizid

Weitere Informationen

Status

  • Quelle:
  • UFAG - Ufficio federale dell'agricoltura. OFAG - Office fédéral de l'agriculture. BLW - Bundesamt für Landwirtschaft.
  • Zulassungsnummer:
  • D-5201
  • Letzte Änderung:
  • 14-11-2018

Packungsbeilage

Handelsbezeichnung: Agroseller Propyzamid-II

(Parallelimport)

Pflanzenschutzmittelverzeichnis (Stand: 06.11.2018)

Produktkategorie:

Ausl. Bewilligungsinhaber:

Eidg. Zulassungsnummer:

Herbizid

Agro Seller Discount AG

D-5201

Stoff(e):

Gehalt:

Formulierungscode:

Wirkstoff: Propyzamide 35.09 % 400 g/l

SC Suspensionskonzentrat

Anwendungen

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

B Freiland: Erdbeere

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 1.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3

Freiland: Rote

Johannisbeere

Freiland: Schwarze

Johannisbeere

Freiland:

Stachelbeere

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3, 4

Freiland: Rote

Johannisbeere

Freiland: Schwarze

Johannisbeere

Freiland:

Stachelbeere

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

2, 3, 4

Kernobst

Steinobst

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Winteranwendung (in der

Vegetationsruhe).

1, 2, 3

O Kernobst

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

2, 3

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

Steinobst

Anwendung: Winteranwendung (in der

Vegetationsruhe).

W Reben

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3, 4

W Reben

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

2, 3, 4

Chicor

[Wurzelproduktion]

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 3.75 l/ha

Anwendung: Nach der Saat oder Pflanzung.

1, 3, 5, 6

G Estragon

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 3.75 l/ha

Wartefrist: 100 Tage

Anwendung: Vorauflauf. W

hrend der

Winterruhe.

1, 3, 6, 7

G Rhabarber

Einj

hrige

Dicotyledonen (Unkr

uter)

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 3.75 l/ha

Anwendung: Oktober - Dezember

1, 3, 6, 8,

mische Kamille

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 3.75 l/ha

Wartefrist: 100 Tage

Anwendung: Anwendung nach der

Pflanzung und nach dem Anwachsen der

Kultur im Herbst oder Anwendung im

Winter w

hrend der Vegetationsruhe oder

Anwendung von M

rz bis Mai auf die

bestehende Kultur.

1, 3, 5, 6,

G Freiland: Salate

(Asteraceae)

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

Aufwandmenge: 2.5 - 3.75 l/ha

Anwendung: Nach der Saat oder Pflanzung.

1, 3, 5

A

Kultur

Schaderreger/

Wirkung

Dosierungshinweise

Auflagen

(Ungr

ser)

G Freiland: Schnittlauch

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2 l/ha

Wartefrist: 45 Tage

1, 3, 6, 10

Raps

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 1.25 - 1.875 l/ha

Anwendung: Nachauflauf Herbst: Stadium

14-16 (BBCH).

1, 3, 11

ume und Str

ucher (ausserhalb

Forst)

Einj

hrige

Dicotyledonen (Unkr

uter)

Einj

hrige

Monocotyledonen

(Ungr

ser)

Aufwandmenge: 2.5 - 4 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

1, 2, 3, 4

ume und Str

ucher (ausserhalb

Forst)

Gemeine Quecke

Aufwandmenge: 5 - 6.25 l/ha

Anwendung: Ab Ende Oktober bis Mitte

Januar.

2, 3, 4

Auflagen und Bemerkungen:

Keine Wirkung auf Klebern und Korbbl

tler wie Franzosenkraut, Kamille und Kreuzkraut.

Auf schnee- und eisfreien Boden.

Ansetzen der Spritzbr

he: Schutzhandschuhe + Schutzanzug tragen. Ausbringen der Spritzbr

he: Schutzhandschuhe + Schutzanzug tragen. Technische Schutzvorrichtungen w

hrend des

Ausbringens (z.B. geschlossene Traktorkabine) k

nnen die vorgeschriebene pers

nliche

Schutzausr

stung ersetzen, wenn gew

hrleistet ist, dass sie einen vergleichbaren oder h

heren Schutz bieten.

Anwendung fr

hestens 6 Monate nach Pflanzung.

Bei geringen Niederschl

gen und in trockenen Gebieten muss das Produkt nach der Applikation

eingeregnet werden.

Bewilligt als geringf

gige Verwendung nach Art. 35 PSMV (minor use).

Anwendung nur in Kulturen zur Produktion von

therischen Ölen f

r die Kosmetikindustrie.

Keine Behandlung im Pflanzjahr.

Behandlung nur w

hrend der vollst

ndigen Winterruhe der Kultur.

10.Behandlung w

hrend der Vegetationsruhe: nach dem Schnitt vor dem erneuten Austrieb.

11.Nach Umbruch von Raps wegen Auswinterung d

rfen keine Getreidearten angebaut werden.

Kartoffeln, R

ben, Erbsen, Bohnen, Sommerraps und Mais sind f

r den Nachbau geeignet.

Gefahrenkennzeichnungen:

Es gilt die Einstufung und Kennzeichnung der ausl

ndischen Originaletikette..

tzliche Schweizerische Gefahrenkennzeichnungen:

SP 1 Mittel und/oder dessen Beh

lter nicht in Gew

sser gelangen lassen.

Im Zweifelsfall gelten einzig die Originaldokumente der Zulassung. Die Erw

hnung eines Produktes,

Wirkstoffes oder einer Firma stellt keine Empfehlung dar und bedeutet nicht, dass sich das Produkt im

Verkauf befindet.

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Cerdelga (Genzyme Europe B.V.)

Cerdelga (Genzyme Europe B.V.)

Cerdelga (Active substance: eliglustat) - Centralised - 2-Monthly update - Commission Decision (2018)3754 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3724/II/15/G

Europe -DG Health and Food Safety

11-6-2018

TAGRISSO (AstraZeneca AB)

TAGRISSO (AstraZeneca AB)

TAGRISSO (Active substance: osimertinib) - Centralised - 2-Monthly update - Commission Decision (2018)3757 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4124/II/19

Europe -DG Health and Food Safety

11-6-2018

Pradaxa (Boehringer Ingelheim International GmbH)

Pradaxa (Boehringer Ingelheim International GmbH)

Pradaxa (Active substance: dabigatran etexilate mesilate) - Centralised - 2-Monthly update - Commission Decision (2018)3755 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/829/II/108

Europe -DG Health and Food Safety

11-6-2018

Xultophy (Novo Nordisk A/S)

Xultophy (Novo Nordisk A/S)

Xultophy (Active substance: insulin degludec / liraglutide) - Centralised - 2-Monthly update - Commission Decision (2018)3779 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2647/II/23

Europe -DG Health and Food Safety

11-6-2018

Bexsero (GlaxoSmithKline Vaccines S.r.l.)

Bexsero (GlaxoSmithKline Vaccines S.r.l.)

Bexsero (Active substance: Meningococcal group B Vaccine (rDNA, component, adsorbed)) - Centralised - 2-Monthly update - Commission Decision (2018)3769 of Mon, 11 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2333/II/59

Europe -DG Health and Food Safety

6-6-2018

Prolia (Amgen Europe B.V.)

Prolia (Amgen Europe B.V.)

Prolia (Active substance: denosumab) - Centralised - 2-Monthly update - Commission Decision (2018) 3685 of Wed, 06 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/1120/II/68

Europe -DG Health and Food Safety

4-6-2018

Yervoy (Bristol-Myers Squibb Pharma EEIG)

Yervoy (Bristol-Myers Squibb Pharma EEIG)

Yervoy (Active substance: ipilimumab) - Centralised - 2-Monthly update - Commission Decision (2018)3618 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2213/II/55

Europe -DG Health and Food Safety

4-6-2018

Eliquis (Bristol-Myers Squibb/Pfizer EEIG)

Eliquis (Bristol-Myers Squibb/Pfizer EEIG)

Eliquis (Active substance: apixaban) - Centralised - 2-Monthly update - Commission Decision (2018)3616 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2148/II/50

Europe -DG Health and Food Safety

4-6-2018

Alecensa (Roche Registration GmbH)

Alecensa (Roche Registration GmbH)

Alecensa (Active substance: alectinib) - Centralised - 2-Monthly update - Commission Decision (2018)3621 of Mon, 04 Jun 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4164/II/10

Europe -DG Health and Food Safety

15-5-2018

CABOMETYX (Ipsen Pharma)

CABOMETYX (Ipsen Pharma)

CABOMETYX (Active substance: cabozantinib) - Centralised - 2-Monthly update - Commission Decision (2018)3015 of Tue, 15 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/4163/II/3

Europe -DG Health and Food Safety

15-5-2018

Repatha (Amgen Europe B.V.)

Repatha (Amgen Europe B.V.)

Repatha (Active substance: evolocumab) - Centralised - 2-Monthly update - Commission Decision (2018)3014 of Tue, 15 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/3766/II/17/G

Europe -DG Health and Food Safety

3-5-2018

Perjeta (Roche Registration GmbH)

Perjeta (Roche Registration GmbH)

Perjeta (Active substance: pertuzumab) - Centralised - 2-Monthly update - Commission Decision (2018)2771 of Thu, 03 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2547/II/35

Europe -DG Health and Food Safety

3-5-2018

Ivemend (Merck Sharp and Dohme Limited)

Ivemend (Merck Sharp and Dohme Limited)

Ivemend (Active substance: fosaprepitant) - Centralised - 2-Monthly update - Commission Decision (2018)2777 of Thu, 03 May 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/743/II/37

Europe -DG Health and Food Safety

5-3-2018

EU/3/16/1789 (La Jolla Pharmaceutical II BV)

EU/3/16/1789 (La Jolla Pharmaceutical II BV)

EU/3/16/1789 (Active substance: Synthetic human hepcidin) - Transfer of orphan designation - Commission Decision (2018)1427 of Mon, 05 Mar 2018 European Medicines Agency (EMA) procedure number: EMA/OD/144/16/T/02

Europe -DG Health and Food Safety

5-3-2018

EU/3/15/1555 (La Jolla Pharmaceutical II BV)

EU/3/15/1555 (La Jolla Pharmaceutical II BV)

EU/3/15/1555 (Active substance: Synthetic hepcidin) - Transfer of orphan designation - Commission Decision (2018)1426 of Mon, 05 Mar 2018 European Medicines Agency (EMA) procedure number: EMA/OD/092/15/T/02

Europe -DG Health and Food Safety