ICI ZITOX 80 WETTABLE POWDER FUNGICIDE

Main information

  • Trade name:
  • ICI ZITOX 80 WETTABLE POWDER FUNGICIDE
  • Class:
  • AgChem
  • Medicine domain:
  • Plants
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • ICI ZITOX 80 WETTABLE POWDER FUNGICIDE
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • APPLE CROP = APPLE ORCHARD | APRICOT | CAPE TULIP | CELERY | CHERRY | NECTARINE | PARSLEY | PEACH | PEAR | PLUM | ROSE | ONELEAF
  • Therapeutic area:
  • FUNGICIDE
  • Therapeutic indications:
  • BLACK SPOT ON ROSE | BLACK SPOT/SCAB IN APPLE/PEAR | BROWN ROT - MONILINIA SPP. | FIRE DISEASE | FRECKLE OR SCAB ON STONE FRUIT | RIPE OR TARGET SPOT ON POME-PEZICULA SPP | SEPTORIA LEAF SPOT - SEPTORIA APIICOLA | SHOTHOLE | STONE FRUIT RUST | APPLE SCAB | BLOSSOM BLIGHT | CELERY LEAF SPOT | CERCOSPORA | CLASTEROSPORIUM | FRECKLE (SCAB) | FRUCTICOLA | GLOEOSPORIUM | LATE BLIGHT | LEAF BLIGHT - S. APIICOLA | PEAR SCAB | PHYLLOS | SHOT HOLE | TRANSZCHELIA PRUNI-SPINOSAE | VENTURIA PIRINA

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Archived
  • Authorization number:
  • 30640
  • Last update:
  • 09-08-2016

17-10-2018

Pest categorisation of Stagonosporopsis andigena

Pest categorisation of Stagonosporopsis andigena

Published on: Tue, 16 Oct 2018 00:00:00 +0200 The Panel on Plant Health performed a pest categorisation of Stagonosporopsis andigena, the causal agent of black blight of potato, for the EU. The pest is a well‐defined fungal species and reliable methods exist for its detection and identification. S. andigena is present in Bolivia and Peru. The pest is not known to occur in the EU and is listed in Annex IAI of Directive 2000/29/EC as Phoma andina, meaning its introduction into the EU is prohibited. The ma...

Europe - EFSA - European Food Safety Authority Publications

1-8-2018

Nimenrix (Pfizer Europe MA EEIG)

Nimenrix (Pfizer Europe MA EEIG)

Nimenrix (Active substance: Meningococcal group A, C, W-135 and Y conjugate vaccine) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)5220 of Wed, 01 Aug 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/2226/T/80

Europe -DG Health and Food Safety

16-5-2018

EU/3/03/140 (Novartis Europharm Limited)

EU/3/03/140 (Novartis Europharm Limited)

EU/3/03/140 (Active substance: Tobramycin (inhalation powder)) - Transfer of orphan designation - Commission Decision (2018)3031 of Wed, 16 May 2018 European Medicines Agency (EMA) procedure number: EMEA/OD/072/02/T/02

Europe -DG Health and Food Safety