Alembic Pharma gets USFDA nod for generic version of Tamiflu capsules Farhat Nasim25 Jun 2019 11:54 AM ISTThe approved product, Oseltamivir Phosphate capsule is therapeutically equivalent to the reference listed drug (RLD), Tamiflu Capsules of Hoffman-La...
Indian Immunologicals invests Rs 75 crore to set up new Sterile Filling Facility in Telangana Farhat Nasim25 Jun 2019 11:36 AM ISTWith this investment of Rs 75 crores in the upcoming filling facility, Indian Immunologicals Limited expects to increase its capacity to supply...
Dr Reddys unveils generic version of Vitamin K1 injection in US Medical Dialogues Bureau25 Jun 2019 10:52 AM ISTThe Vitamin K1 (Phytonadione) for Injectable Emulsion USP, 10 mg/ml brand and generic, had combined US sales of approximately USD 46.6 million MAT for...
Lawsuit: Generic drug makers used code to fix price increases Medical Dialogues Bureau25 Jun 2019 9:15 AM ISTThe alleged conspiracy targeted more than 100 different generic drug(s), including treatments for diabetes, cancer, arthritis and other medical...
Oklahoma judge approves Teva Pharma USD 85 million opioid settlement Medical Dialogues Bureau25 Jun 2019 9:00 AM ISTU.S: An Oklahoma judge on Monday approved a revised $85 million settlement with Teva Pharmaceutical Industries Ltd (Teva Pharma) resolving claims by...
Novartis, Glenmark enter partnership to commercialize, distribute respiratory drugs Seebri, Onbrize, Ultibro Medical Dialogues Bureau24 Jun 2019 3:02 PM ISTUnder the terms of the agreement, Novartis will remain the holder of the registration of the drugs Seebri, Onbrize and Ultibro and will be responsible...
Alembic Pharma gets USFDA nod for Bromfenac Ophthalmic Solution Farhat Nasim24 Jun 2019 12:25 PM ISTThe approved product, Bromfenac Ophthalmic Solution is therapeutically equivalent to the reference listed drug (RLD), Bromday Ophthalmic Solution,...
Dr Reddys gets two USFDA observations for Vizag plants Farhat Nasim24 Jun 2019 11:09 AM ISTHyderabad: City-based Dr Reddy's Laboratories (Dr Reddys/ DRL) has reportedly fallen under the US health regulator's scanner. The company has been...
Glenmark Pharma Ryaltris gets Complete Response Letter from USFDA Medical Dialogues Bureau24 Jun 2019 9:30 AM ISTThe CRL cites deficiencies in the Drug Master File pertaining to one of the active pharmaceutical ingredients and in manufacturing facilities,...
GSK Pharma to optimise product portfolio to drive growth in India Medical Dialogues Bureau24 Jun 2019 9:19 AM ISTGSK is also looking to launch some new products in the country over the next 15 months as it adopts a more structured approach to engage trade channel...
No formal warning issued from AIIMS regarding adverse effects of e-cigarettes: Minister informs Parliament Medical Dialogues Bureau23 Jun 2019 10:15 AM ISTIn response to a question on whether AIIMS has issued any warning regarding harmful effects of e-cigarettes, he said the premier medical institute has...
USFDA declines to approve Daiichi Sankyo blood cancer treatment Quizartinib Farhat Nasim23 Jun 2019 10:00 AM ISTThe decision follows an advisory committee meeting, held in May, where independent advisers to the U.S. regulator voted 8-3 against the drug's...
