FL 200

Main information

  • Trade name:
  • FL 200 10 TAB
  • Pharmaceutical form:
  • TAB
  • Composition:
  • 10
  • Medicine domain:
  • Humans
  • Medicine type:
  • Allopathic drug

Documents

Localization

  • Available in:
  • FL 200 10 TAB
    India
  • Language:
  • English

Other information

Status

  • Source:
  • Central Drugs Standard Control Organization
  • Last update:
  • 09-08-2016

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

20-3-2018

Vietti Foods Issues Allergy Alert on Undeclared Wheat and Eggs in Southgate Hot Dog Chili Sauce

Vietti Foods Issues Allergy Alert on Undeclared Wheat and Eggs in Southgate Hot Dog Chili Sauce

Vietti Foods is recalling approximately 200 cases of 15 oz cans of Southgate Hot Dog Chili Sauce, UPC 0 71846 95242 6, LOT # P642 M1217 70026. This recall has been initiated due to mislabeling because some of the cans may contain Dumplings with Chicken instead of Hot Dog Chili Sauce.

FDA - U.S. Food and Drug Administration

1-3-2018

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company Recalls Select Cases of Its Cherry Ski Product

The Double Cola Company is recalling approximately 200 cases of its Cherry SKI product because they are incorrectly labeled. Only the Cherry SKI products with the new design are being recalled, which were delivered to the southern Illinois, Evansville, IN and Winchester, OH markets.

FDA - U.S. Food and Drug Administration

5-10-2017

Surflink Media and Surflink Media 2 (Models 200 and 210) - used with wireless hearing aids

Surflink Media and Surflink Media 2 (Models 200 and 210) - used with wireless hearing aids

Recall for product correction - may cause interference with mobile towers

Therapeutic Goods Administration - Australia

20-9-2017

Nature Supplement Inc. Issues Voluntary Florida Recall of Vegetable Vigra Due to Undeclared Sildenafil

Nature Supplement Inc. Issues Voluntary Florida Recall of Vegetable Vigra Due to Undeclared Sildenafil

Natures Supplement, Inc. is voluntarily recalling 260 bottles of VEGETABLE VIGRA, 200 mg capsules to the consumer level. FDA analysis found this product to be tainted with Sidenafil. Sildenafil is an FDA approved drug for the treatment of erectile dysfunction, the presence of Sildenafil in the Vegetable Vigra product renders it an unapproved drug for which safety and efficacy has not been established, therefore subject to recall.

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

22-8-2017



Chargenrückruf - Voriconazol Sandoz® 200mg, Filmtabletten

Chargenrückruf - Voriconazol Sandoz® 200mg, Filmtabletten

Swissmedic - Swiss Agency for Therapeutic Products

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

16-6-2017

Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut <sup>tm</sup> (Sodium Bicarbonate 4% Additive Solution), QUELICIN <sup>tm</sup> (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP

Hospira Issues a Voluntary Nationwide Recall For 8.4% Sodium Bicarbonate Injection, USP, Neut <sup>tm</sup> (Sodium Bicarbonate 4% Additive Solution), QUELICIN <sup>tm</sup> (Succinylcholine Chloride Injection, USP) and Potassium Phosphates Injection, USP

Hospira, Inc., a Pfizer company, is voluntarily recalling 42 lots of 8.4% Sodium Bicarbonate Injection, USP, 50 mL vials, 5 lots of NeutTM (Sodium Bicarbonate 4% additive solution) 5 mL vials, 5 lots of QUELICINTM (Succinylcholine Chloride Injection, USP) 200 mg/10 mL vials and 7 lots of Potassium Phosphates Injection, USP, 45 mM vials to the hospital/retail level due to microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of micr...

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

26-5-2017

Astrazeneca Initiates Voluntary Nationwide Recall of One Lot of Brilinta 90 mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle From That Lot

Astrazeneca Initiates Voluntary Nationwide Recall of One Lot of Brilinta 90 mg Professional Sample Bottles Due to Report of Another Medicine in One Bottle From That Lot

AstraZeneca today announced that the Company is notifying physicians and consumers that it is voluntarily recalling one lot of professional (physician) sample bottles containing eight tablets of BRILINTA (ticagrelor) 90mg tablets as a precautionary measure. This voluntary recall follows a report that a professional sample bottle containing eight tablets of BRILINTA 90mg also contained another medicine called ZURAMPIC (lesinurad) 200 mg tablets which is also manufactured by AstraZeneca.

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

17-4-2018

Company Recalls More Than 200 Million Eggs Due to Salmonella Scare

Company Recalls More Than 200 Million Eggs Due to Salmonella Scare

Title: Company Recalls More Than 200 Million Eggs Due to Salmonella ScareCategory: Health NewsCreated: 4/15/2018 12:00:00 AMLast Editorial Review: 4/16/2018 12:00:00 AM

US - MedicineNet

26-2-2018

EU/3/18/1984 (Omeros London Limited)

EU/3/18/1984 (Omeros London Limited)

EU/3/18/1984 (Active substance: Recombinant human monoclonal antibody against mannan-binding lectin-associated serine protease-2) - Orphan designation - Commission Decision (2018)1251 of Mon, 26 Feb 2018 European Medicines Agency (EMA) procedure number: EMA/OD/200/17

Europe -DG Health and Food Safety

21-2-2018

ENDURE 200 (Triclosan) Solution [Ecolab Inc.]

ENDURE 200 (Triclosan) Solution [Ecolab Inc.]

Updated Date: Feb 21, 2018 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

19-12-2017

REVALOR-200 (Trenbolone Acetate And Estradiol) Implant [Merck Sharp Dohme Corp.]

REVALOR-200 (Trenbolone Acetate And Estradiol) Implant [Merck Sharp Dohme Corp.]

Updated Date: Dec 19, 2017 EST

US - DailyMed

14-12-2017

ANTI-AGING FOUNDATION SPF 15 SHADE 200 (Octinoxate) Emulsion [La Prairie, Inc.]

ANTI-AGING FOUNDATION SPF 15 SHADE 200 (Octinoxate) Emulsion [La Prairie, Inc.]

Updated Date: Dec 14, 2017 EST

US - DailyMed

21-11-2017

MOOREBRAND IBUPROFEN (I Buprofen 200 Mg) Tablet, Film Coated [Moore Medical LLC]

MOOREBRAND IBUPROFEN (I Buprofen 200 Mg) Tablet, Film Coated [Moore Medical LLC]

Updated Date: Nov 21, 2017 EST

US - DailyMed

20-11-2017

IBUPROFEN 200MG Tablet, Coated [Athlete'S Needs, Inc.]

IBUPROFEN 200MG Tablet, Coated [Athlete'S Needs, Inc.]

Updated Date: Nov 20, 2017 EST

US - DailyMed

16-11-2017

SOUND BODY IBUPROFEN (Ibuprofen 200 Mg) Capsule, Liquid Filled [Allegiant Health]

SOUND BODY IBUPROFEN (Ibuprofen 200 Mg) Capsule, Liquid Filled [Allegiant Health]

Updated Date: Nov 16, 2017 EST

US - DailyMed

30-10-2017

MUCUS RELIEF (Guaifenesin 200 Mg) Tablet [Richmond Pharmaceuticals, Inc.]

MUCUS RELIEF (Guaifenesin 200 Mg) Tablet [Richmond Pharmaceuticals, Inc.]

Updated Date: Oct 30, 2017 EST

US - DailyMed

18-7-2017

IBUPROFEN 200 (Ibuprofen) Tablet, Coated [Walgreen Company]

IBUPROFEN 200 (Ibuprofen) Tablet, Coated [Walgreen Company]

Updated Date: Jul 18, 2017 EST

US - DailyMed

9-6-2017

TERRAMYCIN 200 GRANULAR (Oxytetracycline) Powder [Phibro Animal Health]

TERRAMYCIN 200 GRANULAR (Oxytetracycline) Powder [Phibro Animal Health]

Updated Date: Jun 9, 2017 EST

US - DailyMed

9-6-2017

TERRAMYCIN 200 (Oxytetracycline) Powder [Phibro Animal Health]

TERRAMYCIN 200 (Oxytetracycline) Powder [Phibro Animal Health]

Updated Date: Jun 9, 2017 EST

US - DailyMed

26-5-2017

CELECOXIB 200 MG (Celecoxib) Capsule [Preferred Pharmaceuticals Inc.]

CELECOXIB 200 MG (Celecoxib) Capsule [Preferred Pharmaceuticals Inc.]

Updated Date: May 26, 2017 EST

US - DailyMed