Food and Drug Administration Newswire (Page 2)

Food and Drug Administration Newswire (Page 2)

Comprehensive Real-Time News Feed for Food and Drug Administration. (Page 2)

Results 21 - 40 of 36,070 in Food and Drug Administration

  1. Most smokers don't stick with e-cigarettesRead the original story w/Photo

    4 hrs ago | KNDU

    ... and last longer than the devices that look more like cigarettes. Earlier this month, the U.S. Food and Drug Administration took action to regulate the e-cigarette industry. Among the measures: The agency said it was banning the sale of e-cigarettes ...

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  2. Salmonella Fast FactsRead the original story w/Photo

    4 hrs ago | CNN

    ... contain at least one type of bacteria that could make you sick, according to their survey. The Food and Drug Administration has issued a ban on some cilantro imported from Mexico after an investigation to determine the cause of hundreds of reported ...

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  3. Lawsuit Claims Gilead Delayed the Release of a Less Toxic Version of TenofovirRead the original story w/Photo

    4 hrs ago | POZ

    ... med. In 2010, research resumed, and in November 2015, the new med received approval from the Food and Drug Administration (FDA). Under the brand name Genvoya, TAF is included in several new combo tablets; however, it is not approved for use as ...

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  4. Can Food Labels Kill Added Sugar?Read the original story w/Photo

    4 hrs ago | Bloomberg

    Sugar is everywhere in the American diet, and now the Food and Drug Administration will begin highlighting just how much of the sweet stuff is added to what we eat. Beginning in July 2018, the "Nutrition Facts" labels on packaged foods will list added sugars separately from total sugars.

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  5. City of Hope Presents New Cancer Research at American Society of Clinical Oncology MeetingRead the original story w/Photo

    4 hrs ago | Business Wire

    ... trial. The treatment combines ixazomib, the first oral proteasome inhibitor approved by the Food and Drug Administration (FDA) in late 2015; pomalidomide, an immunomodulatory agent, and dexamethasone, a steroid that can augment the effects of ...

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  6. FDA Rejects Deutetrabenazine for Treatment of Chorea Associated With Huntington DiseaseRead the original story

    5 hrs ago | P&T Community

    The FDA has issued a complete response letter regarding the new drug application for deutetrabenazine for the treatment of chorea associated with Huntington disease . The agency has asked Teva to examine blood levels of certain metabolites.

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  7. Amarin Announces FDA New Chemical Entity Market Exclusivity...Read the original story w/Photo

    5 hrs ago | Freshnews

    BEDMINSTER, NJ and DUBLIN, IRELAND- - Amarin Corporation plc announced today that the U.S. Food and Drug Administration has determined that Vascepa capsules are eligible for five-year, new chemical entity , marketing exclusivity pursuant to the Hatch-Waxman Amendments to the Federal Food, Drug, and Cosmetic Act. This determination provides Vascepa with the benefits of NCE exclusivity afforded by statute.

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  8. Ocaliva approved for rare liver diseaseRead the original story

    5 hrs ago | UPI

    Ocaliva has been approved by the U.S. Food and Drug Administration to treat a rare chronic liver disease called primary biliary cholangitis . The disease causes the liver's small bile ducts to become inflamed, ultimately destroying the ducts and leading to cirrhosis, which is scarring of the liver.

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  9. On Sale Bar Invalidates Safyral, Beyaz Folate PatentRead the original story w/Photo

    5 hrs ago | JD Supra

    In Merck & CIE v. Watson Laboratories, Inc. , the Federal Circuit found communications between Merck and a potential joint venture partner amounted to a commercial offer to sell that invalidated the Orange Book-listed folate patent at issue.

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  10. Most Smokers Don't Stick With E-CigarettesRead the original story w/Photo

    5 hrs ago | HON

    ... and last longer than the devices that look more like cigarettes. Earlier this month, the U.S. Food and Drug Administration took action to regulate the e-cigarette industry. Among the measures: The agency said it was banning the sale of e-cigarettes ...

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  11. AbbVie, Biogen receive FDA approval for new MS treatmentRead the original story w/Photo

    5 hrs ago | Drug Store News

    The Food and Drug Administration has approved Biogen and AbbVie's Zinbryta , the companies announced Tuesday. The drug is a once-daily self-administered injection indicated to treat relapsing forms of multiple sclerosis in patients who have had an inadequate response to two or more MS therapies.

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  12. Clay country poet suffered from congenital syphilisRead the original story w/Photo

    5 hrs ago | PhysOrg Weblog

    ... beauty clay sold at major retail outlets may put users at risk for lead poisoning, the U.S. Food and Drug Administration warned Friday. Countries that implement government-mandated vaccinations for chickenpox see a sharp drop in the number of Google ...

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  13. Radius Announces FDA Acceptance for Filing of New Drug Application...Read the original story

    5 hrs ago | GlobeNewswire

    Radius Health, Inc. , a science-driven biopharmaceutical company that is committed to developing innovative therapeutics in the areas of osteoporosis, oncology and endocrine diseases, today announced that its New Drug Application for abaloparatide-SC has been accepted for filing by the U.S. Food and Drug Administration . The acceptance of the NDA reflects the FDA's determination that the application is sufficiently complete to permit a substantive review.

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  14. Depression and Botox: Clinical Research Trials Show PromiseRead the original story w/Photo

    8 hrs ago | PR Log

    ... or a co-pay, and no bill is issued. All medical research occurs under the guidelines of the Food and Drug Administration as well as oversight of an ethical review committee. For more information, call 770-817-9200. About the Institute for Advanced ...

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  15. FDA Releases Final Guidance Regarding the Food Labeling Term "Evaporated Cane Juice"Read the original story w/Photo

    9 hrs ago | jdsupra.com

    The US Food and Drug Administration has released final guidance stating its view that sweeteners derived from sugar cane should not be declared in the statement of ingredients as "evaporated cane juice." FDA's view is that the term "evaporated cane juice" is false or misleading because it suggests that the sweetener is fruit or vegetable juice or is made from fruit or vegetable juice, and does not reveal that the ingredient's basic nature and characterizing properties are those of a sugar.

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  16. First FDA Cleared Procedure for Tissue Regeneration Utilizes Laser...Read the original story w/Photo

    10 hrs ago | PRWeb

    ... with Dr. Peavy at his practice. The LANAP protocol is now the world's first to receive Food and Drug Administration (FDA) clearance for True Regenerationa . Patients with gum disease can now receive the only laser periodontal therapy treatment ...

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  17. Vertex Release: FDA Accepts For Priority Review Supplemental New Drug ...Read the original story

    Monday | BioSpace

    Vertex Pharmaceuticals Incorporated today announced that the U.S. Food and Drug Administration has accepted for review a supplemental New Drug Application for the use of ORKAMBIA in people with cystic fibrosis ages 6 to 11 who have two copies of the F508del mutation. The FDA granted Vertex's request for Priority Review of this sNDA, and a target review date of September 30, 2016 was set under the Prescription Drug User Fee Act .

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  18. FDA Grants QIDP And Fast Track Designation To CD101 Topical, Cidara...Read the original story

    Monday | BioSpace

    Cidara Therapeutics, Inc. , a biotechnology company developing novel anti-infectives and immunotherapies to treat fungal and other infections, today announced that the U.S. Food and Drug Administration has designated the company's novel antifungal product candidate, CD101 topical, as a Qualified Infectious Disease Product , with Fast Track status for its development program. The designation is for the development of CD101 for the treatment of vulvovaginal candidiasis and for the prevention of recurrent VVC .

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  19. Us Fda warns CordenPharma about Italian antibiotic Api and cancer injectables plantRead the original story w/Photo

    Monday | Drug Researcher

    The US FDA was warned CordenPharma about manufacturing operations at a plant in Italy that was approved to make injectable cancer drugs last year. CordenPharma said it had been warned by the Food and Drug Administration last week.

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  20. Celebrating a Year of the Expedited Access Pathway Program for Medical DevicesRead the original story w/Photo

    Tuesday May 3 | US Food and Drug Administration

    The U.S. Food and Drug Administration is committed to supporting patient access to high-quality, safe, and effective medical devices of public health importance - as quickly as possible. Erin Cutts, B.S., Policy Lead, Q-Submission Program , Office of Device Evaluation in FDA's Center for Devices and Radiological Health For patients suffering from life-threatening conditions and who have few, if any, options, this access becomes critical.

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