GESAMIL 500 WETTABLE POWDER SELECTIVE HERBICIDE

Main information

  • Trade name:
  • GESAMIL 500 WETTABLE POWDER SELECTIVE HERBICIDE
  • Class:
  • AgChem
  • Medicine domain:
  • Plants
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • GESAMIL 500 WETTABLE POWDER SELECTIVE HERBICIDE
    Australia
  • Language:
  • English

Therapeutic information

  • Therapeutic group:
  • BROAD BEAN | CANNING PEA | CARROT | FIELD PEA | LUPIN | PARSNIP | FABA BEAN | ROOT
  • Therapeutic area:
  • HERBICIDE
  • Therapeutic indications:
  • ANNUAL OR WIMMERA RYEGRASS | BLACKBERRY NIGHTSHADE | CAPEWEED | CHARLOCK | CHICKWEED | COBBLER'S PEGS | CORN GROMWELL, IRONWEED OR SHEEPWEED | CORN SPURRY | DEADNETTLE | FAT HEN | FUMITORY | GREEN AMARANTH | HEDGE OR WILD MUSTARD | INDIAN HEDGE MUSTARD | LESSER SWINECRESS OR BITTERCRESS | PATERSON'S CURSE | PERENNIAL PIGWEED | PLANTAIN | POTATO OR YELLOW WEED | PRAIRIE OR ANNUAL PRAIRIE GRASS | REDSHANK,SLIM OR SPLEEN AMARANTH | SHEPHERD'S PURSE | SOW OR MILK THISTLE | STAGGER WEED | STINGING OR DWARF NETTLE | STINKING ROGER | WILD RADISH OR RADISH WEED | WILD TURNIP | WINTER GRASS | WIREWEED, KNOTWEED OR HOGWEED | AMARANTHUS CRUENTUS | ANNUAL BLUE GRASS | ANNUAL DWARF NETTLE | ANNUAL NETTLE | ANNUAL POA | BLACK NIGHTSHADE | BRASSICA CAMPESTRIS | BRASSICA KABER | BRASSICA RAPA SSP. SYLVESTRIS | BRASSICA RAPA VAR. SYLVESTRIS | BRASSICA SINAPISTRUM | BROMUS CATHARTICUS | BROMUS STAMINEUS | BROMUS WILDENOWII | BUGLOSSIODES ARVENSE | COMMON CHICKWEED | COMMON PLANTAIN | COMMON SOWTHISTLE | CONYZA SPP. | CRAMBLING

Other information

Status

  • Source:
  • Australian Pesticides and Veterinary Medicines Authority (APVMA)
  • Authorization status:
  • Archived
  • Authorization number:
  • 31830
  • Last update:
  • 09-08-2016

13-7-2018

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions

Hospira Issues Voluntary Nationwide Recall of Daptomycin for Injection Lyophilized Powder for Solution, Due to Infusion Reactions

Hospira, Inc., a Pfizer company, is voluntarily recalling 8 lots of Hospira’s Daptomycin for Injection 500 mg, Lyophilized Powder For Solution, Single Dose Vial (NDC 0409-0106-01) to the Hospital/Retail level. The product is being recalled due to adverse event reports indicative of infusion reactions.

FDA - U.S. Food and Drug Administration

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