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  • KemPharm, Inc. announced that the New Drug Application (NDA) for KP201/APAP, its investigational drug candidate for the short-term management of acute pain, has been accepted and granted priority review by the U.S. Food and Drug Administration (FDA).  In addition, the FDA has set a target action date under the Prescription Drug User Fee Act (PDUFA) of June 9, 2016.

  • Aurobindo Pharma Limited announce that the company has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Levofloxacin in 5% Dextrose Injection, 250 mg/50 mL (5 mg/mL), 500 mg/100 mL (5 mg/mL), and 750 mg/150 mL (5 mg/mL), single-use containers. The product is expected to be launched in Q1 FY16-17. The approved ANDA is bioequivalent and therapeutically equivalent to the reference listed drug product (RLD) Levaquin® (Levaquin in 5 % Dextrose) by Janssen Pharmaceuticals, Inc.

  • After the age of nine months, the development of the infant gut microbiota is driven by diet, not maternal obesity, a new study says.The gut microbiota is a complex community of microorganisms that live in the digestive tract.

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  • Feeding fish oil-based diet for three weeks has been found to slow progression of Alzheimer's like symptoms in mouse models of the disease, reports a new study, supporting viability of a dietary approach to combat the brain disorder in humans.

  • Researchers have found that a US Food and Drug Administration (FDA)-approved drug currently used for obese patients and Type-2 diabetics has the potential to be used in the treatment of cocaine dependence.

  • British researchers have identified a key protein that can control how breast cancer cells spread in the body.The study sheds light on how cancer cells leave the blood vessels to travel to a new part of the body, said the researchers from University of Manchester in Britain.

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