Search results for digitek

In an April 28, 2008 MedWatch Safety Alert about Digitek (digoxin tablets), the FDA informed doctors and patients that this prescription medication is the subject of a nationwide Class I recall. read more »
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The facts surrounding the late April 2008 recall of Digitek (digoxin) pills that may have twice the active ingredient is becoming less clear as we learn more in the days following the FDA recall. read more »
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Heart Medication Sold By Mylan Was Made In Actavis Plant That Received FDA Letter About Manufacturing Problems Over A Year Ago read more »
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North Carolina Board Of Pharmacy Has Posted A Copy Of The Bertek Digitek Drug Recall Notice On Its Web Site read more »
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Actavis, Mylan, Or The FDA Should Tell Public Their Current Estimate Of How Many Defective Digitek Pills Were Distributed To Pharmacies, And During What Time Period read more »
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June 2008 Recall By ETHEX Is Similar To Digitek Recall, But Here The Drug Company Is Able To Provide Specific Information About Dates And Lot Numbers, Unlike Actavis read more »
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FDA Statement Suggests Actavis Will Be Held Accountable For The Defective Digitek Pills, And Mylan Maintains That This Is Not My(lan) Problem read more »
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Judge Joseph R. Goodwin Will Preside Over "Double-Dose" Digitek Pill Cases Pursuant To MDL Litigation Order read more »
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After Earlier Class 1 Recall Of Digitek, All Acvtavis Drugs Manufactured At Its Little Falls, NJ Plant Were Recalled In August 2008 read more »
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Federal Government Seeks A Permanent Injunction Against This Drug Company That Produced Defective Digitek (Digoxin) Pills read more »
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