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Cans of a popular, ready-to-drink weight loss product are being recalled in the United States after tests showed the liquid meals could be tainted with bacteria, the Food and Drug Administration said Friday.
SAN DIEGO----Santarus, Inc. , a specialty biopharmaceutical company, today announced that the U.S. Food and Drug Administration has approved the company’s New Drug Application for immediate-release omeprazole/sodium bicarbonate/ magnesium hydroxide tablets in 40 mg and 20 mg dosage strengths of omeprazole.
Pharmaceutical company AstraZeneca PLC said Friday it has won U.S. approval for use of its schizophrenia drug Seroquel XR as an add-on treament for major depressive disorder.
Biotech reporter Adam Feuerstein answers reader email about Hemispherx Biopharma, Cel-Sci and other stocks.
The U.S. Food and Drug Administration warned Longview-based Cloud's Food Service for public health violations its inspectors found this summer.
Eleven journalism organizations are urging the Food and Drug Administration to end practices that they contend restrict the public’s access to information.
MENTOR, Ohio----STERIS Corporation was notified on December 3, 2009 that the U.S. Food and Drug Administration had issued a notice to healthcare facility administrators regarding the regulatory status of the STERIS SYSTEM 1® Sterile Processing System, as well as actions healthcare facilities should take if they use this device.
Stung by the continuing struggle to make a vaccine against the swine flu pandemic, Health and Human Services Secretary Kathleen Sebelius said on Tuesday her department would review its approach to disaster preparedness.
WASHINGTON -- Regulators have shut down big Ohio bank AmTrust Bank.
Obama plans new jobs bill to 'jump-start' hiring, sees 'better days' ahead for employment
ENGLEWOOD CLIFFS, N.J. (AP) - All canned Slim Fast drinks are being voluntarily recalled by the company over fears of bacterial contamination that could cause diarrhea, nausea and vomiting. The recall affects all 10 million products currently on the market.
The Food and Drug Administration urged health care providers to find substitutes for a key Steris product because the piece of sterilization equipment no longer has FDA approval.
Drugmakers, FDA move to curb painkiller abuse
The US Food and Drug Administration (FDA) sent a warning letter to the company following an inspection in August at what it said was the seafood soup manufacturing facility in Fort Worth.
The U.S. Food and Drug Administration today approved Zyprexa® in tablet form as an option for the treatment of schizophrenia and manic or mixed episodes associated with bipolar I disorder in adolescents aged 13-17 years old.
WASHINGTON, Dec.
