Aurobindo Pharma gets USFDA nod for Azithromycin 250 mg and 500 mg Medical Dialogues Bureau24 Feb 2020 2:22 PM ISTNew Delhi: Drug firm Aurobindo Pharma has received final approval from the USFDA to manufacture and market Azithromycin tablets, used for the...
USV not dominant player, hence no case: CCI dismisses petition by pharma wholesaler MD bureau24 Feb 2020 1:23 PM ISTNew Delhi: Noting that the drug firm USV does not seem to enjoy the dominant position in the portfolio of medicines that it sells and hence no case...
Coronavirus: Restrictions imposed on the export of medical equipment to China Medical Dialogues Bureau24 Feb 2020 12:29 PM ISTNew Delhi: India said some restrictions were imposed on export of certain medical equipment to China in view of their short supply within the country...
Solara Puducherry and Mangalore facilities complete USFDA Inspection with zero 483s observations Medical Dialogues Bureau24 Feb 2020 12:18 PM ISTChennai: Solara Active Pharma Science Limited (Solara), an active Pharmaceutical Ingredient provider has announced that the US Food and Drug...
Biocon's Insulin Manufacturing Facility in Malaysia Completes USFDA inspection with three observations Medical Dialogues Bureau24 Feb 2020 12:11 PM ISTMalaysia:Drug major Biocon recently informed about the USFDA inspection at its Insulin Manufacturing Facility in Malaysia, and that the agency issued...
USFDA approves Eli Lilly's Trulicity (dulaglutide) for reduction in MACE in type 2 diabetes patient Medical Dialogues Bureau23 Feb 2020 12:00 PM ISTNew indication reflects a distinct patient population in the REWIND study, including primary people with multiple cardiovascular risk factors but...
AIIMS director kickstarts three day International Conference at Delhi Pharmaceutical Sciences and Research University Medical Dialogues Bureau23 Feb 2020 12:00 PM ISTNew Delhi: Delhi Pharmaceutical Sciences and Research University (DPSRU) is hosting a three day International Conference of Cardiovascular Sciences-...
Following SC orders, CDSCO asks Pharma manfacturers submit data on 66 fixed-dose combinations MD bureau23 Feb 2020 11:45 AM ISTNew Delhi: In continuation of the series of directives that the FDC Division, Central Drugs Standard Control Organization (CDSCO), Directorate General...
FDA approves Lundbeck's intravenous migraine prevention drug Vyepti, to launch in April 2020 Medical Dialogues Bureau23 Feb 2020 11:30 AM ISTDeerfield: Lundbeck announced that VYEPTI™ (eptinezumab-jjmr) has been approved by the U.S. Food and Drug Administration (FDA) for the preventive...
Heron Therapeutics Announces FDA Extension of Review Period for NDA for HTX-011 for Management of Postoperative Pain Medical Dialogues Bureau23 Feb 2020 9:30 AM ISTSAN DIEGO : Heron Therapeutics, Inc,. a commercial-stage biotechnology company focused on improving the lives of patients by developing...
Strides Consumer forays into North India market Medical Dialogues Bureau22 Feb 2020 4:29 PM ISTAs part of the foray, the company has launched two products -- Nixit, and oral nicotine replacement therapy (NRT) product, and Jointflex, a topical...
With USFDA approval in Hand, Esperion to launch Non-Statin Cholesterol drug NEXLETOL for as low as 10 dollars Medical Dialogues Bureau22 Feb 2020 4:10 PM ISTEligible patients in the USA with commercial drug insurance coverage for NEXLETOL may pay as little as $10 per fill, up to a 3-month supply.
