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Gland Pharma announced that it has received final approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug Application (ANDA) for Vasopressin in 5% Dextrose ...
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Capital Market on MSNGland Pharma receives USFDA approval for Vasopressin in 5% Dextrose RTU Injection
Gland Pharma has received approval from the United States Food and Drug Administration (USFDA) for its Abbreviated New Drug ...
Doctors say hormone therapy is a great option for many, but not all, menopausal women — and it's important to understand the ...
The FDA is warning that nitrous oxide, commonly known as “laughing gas," is being misused as a recreational drug.
A Jacksonville seafood company voluntarily recalled a frozen raw shrimp product over possible radioactive contamination, ...
“This is the first human case of travel-associated New World screwworm myiasis (parasitic infestation of fly larvae) from an ...
The decision seemingly contradicts the Office of Personnel Management’s guidance not to terminate collective bargaining ...
The recall is currently categorized as Class II by the FDA, meaning that use of the product “may cause temporary or medically ...
Some Moo-llennium Crunch Ice Cream half gallons were packaged in Chocolate Chip Cookie Dough cartons, posing a risk for those ...
The Department of Health and Human Services reported the first human case of New World Screwworm in the U.S. The diagnosis ...
The Food and Drug Administration (FDA) has expanded the approval of Repatha ® (evolocumab) to include use in adults at increased risk for major adverse cardiovascular events (MACE) due to uncontrolled ...
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