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Wockhardt ends weak despite US FDA nod for generic drug19-NOV-09
Wockhardt closed at Rs 175, lower by Rs 5 or 2%, on the BSE.
Wockhardt gets FDA nod for Nicardipine injections18-NOV-09
Drug firm Wockhardt today said it has received the final approval from the US Food and Drug Administration (FDA) for marketing Nicardipine HCI injections in 25mg/10 ml strength, used in the treatment of hypertension.
Sun Pharma gets tentative FDA nod for generic Gleevec tablets17-NOV-09
Sun Pharmaceutical Industries today said it has got tentative approval from the US drug regulator for generic Gleevec (imatinib meyslate tablets), used in the treatment of chronic myeloid leukaemia.
Glenmark up on US FDA nod for dermatological cream16-NOV-09
The stock finally ended with a gain of 3.5% at Rs 230 as against the day's high of Rs 238. Around 487,310 shares changed hands at the counter on the BSE today.
Reametrix scouts for strategic partners16-NOV-09
Reametrix, a Bangalore-based company that provides basic research and assay development services to biotechnology and pharmaceutical companies, is scouting for strategic partners to take TriTstat, a critical diagnostic product for managing HIV patients, to the global markets.
Glenmark Generics gets US FDA nod for Ciclopirox Olamine14-NOV-09
Glenmark Generics today said it has received ANDA (abbreviated new drug application) approval from the United States Food and Drug Administration for Ciclopirox Olamine cream, used in the treatment of dermatological infections.
India Eco Summit: Issues with USFDA to drag on, says Ranbaxy09-NOV-09
Pharmaceutical firm Ranbaxy today said it is in talks with the US Food and Drug Administration (USFDA)to sort out issues related to generic drugs but the matter is likely to take long to resolve.
Caraco looking at shifting production to India02-NOV-09
Also considering selling some of its third-party products.
USFDA tells Glenmark to withdraw drug15-OCT-09
The US Food and Drug Administration (FDA) has directed Glenmark's US arm, Glenmark Generics Inc, and three other manufacturers to stop the marketing of unapproved codeine sulphate tablets in the US market. The drug is an old narcotics product widely used to treat pain.
Exclusivity gains05-OCT-09
While the FDA approval for an antibiotic should improve revenue visibility and help Orchid Chemicals reduce debt, the upsides are priced in.
Aurobindo gets US FDA nod19-SEP-09
Aurobindo Pharma Limited has received the tentative approval for Atomoxetine Hydrochloride capsules in 10mg, 18mg, 25mg, 40mg, 60mg, 80mg, and 100mg strengths.
Glenmark gets US FDA nod for hypertension drug18-SEP-09
Drug maker Glenmark Generics, a group firm of Glenmark Pharmaceuticals, has received approval from the US drug regulator for its anti-hypertension tablets.
Sun, Caraco to file 30 marketing applications for generics17-SEP-09
Sun Pharmaceutical Industries and its troubled US subsidiary, Caraco Pharmaceuticals, plan to together file 30 Abbreviated New Drug Applications with the US Food and Drug Administration (FDA) to market generic drugs, despite regulatory issues for the US company.
Suven Life gets two more US patents for NCEs14-SEP-09
Suven Life Sciences Limited, a Hyderabad-based biopharmaceutical company specialising in central nervous system (CNS) diseases, has received patents for two new chemical entities (NCEs) from the US Patent office.
US FDA say GSK vaccine blocks cancer virus05-SEP-09
The US Food and Drug Administration says a vaccine from GlaxoSmithKline successfully blocks the virus that causes most cases of cervical cancer.
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