Danacetat 75 fl.

Primær information

  • Handelsnavn:
  • Danacetat 75 fl. Vandopløseligt koncentrat
  • INN (International Name):
  • MCPA
  • Lægemiddelform:
  • Vandopløseligt koncentrat
  • Sammensætning:
  • 750 g/l MCPA
  • Brugt til:
  • Planter
  • Medicin typen:
  • agrokemiske

Dokumenter

  • for den brede offentlighed:
  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.


    Anmode informationsbrochure for offentligheden.

  • for sundhedspersonale:
  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.


    Anmode informationsbrochure for sundhedspersonale.

Lokation

  • Fås i:
  • Danacetat 75 fl. Vandopløseligt koncentrat
    Danmark
  • Sprog:
  • dansk

Andre oplysninger

Status

  • Kilde:
  • SEGES Landbrug & Fødevarer
  • Autorisation status:
  • Udgået
  • Autorisationsnummer:
  • 14-225
  • Sidste ændring:
  • 07-02-2018
  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.

    Anmode informationsbrochure for offentligheden.

13-4-2018

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group Issues Allergy Alert on Undeclared Sulfites in La Marinera Brand Dried Yellow Potatoes

Guixens Food Group, Inc., of Miami, FL, is voluntarily recalling its ten-ounce packages of La Marinera Brand Dried Yellow Potatoes because it may contain undeclared sulfites. People who have an allergy or severe sensitivity to sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.

FDA - U.S. Food and Drug Administration

9-4-2018

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk

Club 13 of St. Augustine, FL is recalling 15-gram, 30-gram, 90-gram, 150-gram, and 454-gram pouches, and all bulk orders of "Maeng Da Red" kratom powder; and 5-count, 25-count, 50-count, 100-count, 120-count capsule, and all bulk capsule orders of “Maeng Da Red” kratom bottles; and 5-count, 20-count, 25-count, 40-count, 50-count capsule “Maeng Da Red XS” kratom bottles because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections i...

FDA - U.S. Food and Drug Administration

11-1-2018

Clopidogrel Tablets USP, 75 mg by International Laboratories: Recall - Product Mislabeling

Clopidogrel Tablets USP, 75 mg by International Laboratories: Recall - Product Mislabeling

Missed doses of Clopidogrel increases the risk of heart attack and stroke which can be life threatening.

FDA - U.S. Food and Drug Administration

10-1-2018

International Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel Tablets USP, 75 mg packaged in bottles of 30 tablets Due to Mislabeling NDC # 54458-888-16; Lot # 117099A

International Laboratories, LLC Issues Voluntary Nationwide Recall of one (1) Lot of Clopidogrel Tablets USP, 75 mg packaged in bottles of 30 tablets Due to Mislabeling NDC # 54458-888-16; Lot # 117099A

International Laboratories, LLC is voluntarily recalling Lot# 117099A of Clopidogrel Tablets, USP 75 mg, packaged in bottles of 30 tablets, to the consumer level due to mislabeling. The product is labeled as Clopidogrel tablets USP 75 mg but may contain Clopidogrel 75mg or Simvastatin Tablets USP 10 mg.

FDA - U.S. Food and Drug Administration

23-8-2017

Centurion Labs Issues Voluntary Nationwide Recall of Ninjacof (Lot # 200N1601) and Ninjacof A (Lot# 201NA1601) Products Due to Potential <em>Burkholderia Cepacia</em> Contamination

Centurion Labs Issues Voluntary Nationwide Recall of Ninjacof (Lot # 200N1601) and Ninjacof A (Lot# 201NA1601) Products Due to Potential <em>Burkholderia Cepacia</em> Contamination

Centurion Labs is voluntarily recalling, as a precautionary measure, 1 lot of Ninjacof (Lot# 200N1601) and 1 lot of Ninjacof A (Lot# 201NA1601) manufactured by Vilvet (Dania Beach, FL) and distributed by Centurion Labs to the retail level due to potential contamination with Burkholderia cepacia. Centurion was notified by the FDA regarding the potential contamination as they discovered this product may have been manufactured in a Pharmatech, FDA registered facility, in Davie, FL. that was found to have a ...

FDA - U.S. Food and Drug Administration

3-8-2017

Rugby Laboratories Issues Voluntary Nationwide Recall of Diocto Liquid and Diocto Syrup Manufactured By PharmaTech, LLC Due to Possible Product Contamination

Rugby Laboratories Issues Voluntary Nationwide Recall of Diocto Liquid and Diocto Syrup Manufactured By PharmaTech, LLC Due to Possible Product Contamination

Rugby® Laboratories of Livonia, MI is voluntarily recalling all lots within the expiry of Diocto Liquid and Diocto Syrup, (docusate sodium solutions) manufactured by PharmaTech, LLC of Davie, FL due to a risk of product contamination with Burkholderia cepacia. If a product contains B. cepacia, its use could result in infections in patients with compromised immune systems and in patients with chronic lung conditions such as cystic fibrosis. Some of these infections may be serious or even life-threatening ...

FDA - U.S. Food and Drug Administration

5-6-2017

Global Garlic Inc. Recalls "Queso Freso/Whole Milk Cheese" Because of Possible Health Risk

Global Garlic Inc. Recalls "Queso Freso/Whole Milk Cheese" Because of Possible Health Risk

Global Garlic Inc., 11501 NW 107th ST, Miami, FL, is recalling its 16oz packages of “Queso Fresco/ Whole Milk” and (“Queso Fresco x LB(Barra)/Whole Milk Cheese” because they have the potential to be contaminated with Listeria monocytogenes, and organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, na...

FDA - U.S. Food and Drug Administration

29-5-2017

Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas&#8482; 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information

Lupin Pharmaceuticals Inc. Announces a Nationwide Recall of Mibelas&#8482; 24 Fe (Norethindrone Acetate and EthinylEstradiol 1mg/0.02mg Chewable Tablets and Ferrous Fumarate 75 mg) Tablets Due to Out of Sequence Tablets and Missing Expiry/Lot Information

Baltimore, Maryland, Lupin Pharmaceuticals Inc. announced today that it has voluntarily recalled lot L600518, Exp 05/18 of Mibelas 24 Fe (Norethindrone Acetate and Ethinyl Estradiol 1 mg/0.02 mg chewable and ferrous fumarate 75 mg) Tablets at the consumer level. A confirmed market complaint indicated a packaging error, where the blister was rotated 180 degrees within the wallet, reversing the weekly tablet orientation and making the lot number and expiration date no longer visible. The first four days of...

FDA - U.S. Food and Drug Administration

18-5-2017

La Nica Products, Inc. Retira Queso Por Posible Riesgo De Salud

La Nica Products, Inc. Retira Queso Por Posible Riesgo De Salud

La Nica Products, Inc. de Miami, FL está retirando seis mil libras de queso, ya que puede estar contaminada con Listeria monocytogenes, un organismo que puede causar infecciones graves y a veces fatales en niños pequeños, personas débiles o ancianas y otros con sistemas inmunológicos debilitados. Las personas sanas pueden sufrir síntomas de corto plazo como fiebre alta, dolor de cabeza intenso, rigidez, náuseas, dolor abdominal y diarrea, infección por listeria puede causar abortos espontáneos y mortinat...

FDA - U.S. Food and Drug Administration

16-5-2017

La Nica Products, Inc. Recalls Cheese Because of Possible Health Risk

La Nica Products, Inc. Recalls Cheese Because of Possible Health Risk

La Nica Products, Inc. of Miami, FL is recalling six thousand pounds of cheese, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and sti...

FDA - U.S. Food and Drug Administration

7-10-2016

Experts for the European Pharmacopoeia's groups of experts and working parties

Experts for the European Pharmacopoeia's groups of experts and working parties

A very large part of the work related to the drafting of new monographs for the European Pharmacopoeia (EDQM) is carried out by external experts in 75 groups of experts and working parties. Experts for the groups are appointed for a period of three years, and the EDQM is now seeking experts for the period from 2017 to 2019.

Danish Medicines Agency

10-4-2018

RoActemra (Roche Registration GmbH)

RoActemra (Roche Registration GmbH)

RoActemra (Active substance: tocilizumab) - Centralised - Transfer Marketing Authorisation Holder - Commission Decision (2018)2179 of Tue, 10 Apr 2018 European Medicines Agency (EMA) procedure number: EMEA/H/C/955/T/75

Europe -DG Health and Food Safety

19-3-2018

RANITIDINE 75 MG (Ranitidine) Tablet, Film Coated [Vivimed Labs Limited]

RANITIDINE 75 MG (Ranitidine) Tablet, Film Coated [Vivimed Labs Limited]

Updated Date: Mar 19, 2018 EST

US - DailyMed

28-12-2017

ZANTAC 75 (Ranitidine) Tablet, Coated [Carilion Materials Management]

ZANTAC 75 (Ranitidine) Tablet, Coated [Carilion Materials Management]

Updated Date: Dec 28, 2017 EST

US - DailyMed

22-12-2017

VITAL-FL (Body Fluid Balance) Liquid [Vitaltiy Works, Inc.]

VITAL-FL (Body Fluid Balance) Liquid [Vitaltiy Works, Inc.]

Updated Date: Dec 22, 2017 EST

US - DailyMed

8-12-2017

RANITIDINE 75 (Ranitidine Tablets) Tablet [Meijer Distribution Inc]

RANITIDINE 75 (Ranitidine Tablets) Tablet [Meijer Distribution Inc]

Updated Date: Dec 8, 2017 EST

US - DailyMed

8-12-2017

RANITIDINE 75 (Ranitidine Tablets Usp, 75mg) Tablet [The Kroger Co.]

RANITIDINE 75 (Ranitidine Tablets Usp, 75mg) Tablet [The Kroger Co.]

Updated Date: Dec 8, 2017 EST

US - DailyMed

28-11-2017

ACID REDUCER 75 (Ranitidine 75mg) Tablet, Coated [Allegiant Health]

ACID REDUCER 75 (Ranitidine 75mg) Tablet, Coated [Allegiant Health]

Updated Date: Nov 28, 2017 EST

US - DailyMed

26-10-2017

Ingelvac CircoFLEX (Boehringer Ingelheim Vetmedica GmbH)

Ingelvac CircoFLEX (Boehringer Ingelheim Vetmedica GmbH)

Ingelvac CircoFLEX (Active substance: Porcine circovirus type 2 ORF2 protein minimum RP1.0 Maximum RP 3.75) - Centralised - Yearly update - Commission Decision (2017)7264 of Thu, 26 Oct 2017

Europe -DG Health and Food Safety

2-10-2017

Current standards applicable to TGA-licensed HPC manufacturers

Current standards applicable to TGA-licensed HPC manufacturers

TGO 94 Standard for HPCs derived from Cord Blood has replaced TGO 75

Therapeutic Goods Administration - Australia

25-9-2017

ZANTAC 75 (Ranitidine) Tablet [JC World Bell Wholesale Co., Inc.]

ZANTAC 75 (Ranitidine) Tablet [JC World Bell Wholesale Co., Inc.]

Updated Date: Sep 25, 2017 EST

US - DailyMed