Apr 30, 2016 at 13:16 | Source: PTI
"National Pharmaceutical Pricing Authority (NPPA) has fixed/revised ceiling prices of 54 scheduled formulations of Schedule-I under Drugs (Price Control) Amendment Order, 2016 and retail price of two formulations under DPCO, 2013," the regulator said in a statement.
Apr 29, 2016 at 14:56 | Source: PTI
In 2013, government had constituted a high level committee headed by V M Katoch to study the whole issue of active pharmaceutical ingredients (APIs) of critical importance.
Apr 29, 2016 at 14:08 | Source: PTI
"The company has received final approval from the US Food & Drug Administration (USFDA) to manufacture and market Lacosamide tablets, 50 mg, 100 mg, 150 mg and 200 mg," Aurobindo Pharma said in a filing on BSE.
Apr 29, 2016 at 12:46 | Source: PTI
"Glenmark Pharmaceuticals, USA, has been granted tentative approval by the US Food and Drug Administration (USFDA) for adapalene and benzoyl peroxide gel, 0.1 percent/ 2.5 percent," it said in a BSE filing today.
Apr 29, 2016 at 09:42 | Source: PTI
The company had acquired oral methylergonovine maleate (Methergine) earlier this year, Lupin said in a statement.
Apr 29, 2016 at 07:38 | Source: PTI
In a regulatory filing, Granules India said its Board of Directors today "approved further investment of USD 17.07 million (about Rs 117 crore) by way of debt/equity in Granules Pharmaceutical Inc, a wholly-owned foreign subsidiary of the company."
Apr 28, 2016 at 09:54 | Source: PTI
The tablets in the strength of 80 mg are made by Torrent for its US arm Torrent Pharma Inc, the latest US Food and Drug Administration (USFDA) enforcement report said.
Apr 28, 2016 at 09:52 | Source: PTI
Citing a number of issues, including quality control, the US health regulator said it "may withhold approval of any new applications or supplements listing your firm as drug manufacturer" till corrections were made by the company which has been placed on import alert on September 11, 2015.
Apr 28, 2016 at 07:38 | Source: PTI
Wyeth, the unit, was accused of knowingly reporting to the government false and fraudulent prices for two forms of Protonix, a drug notably used to treat symptoms of acid reflux, from 2001 at 2006, before it was acquired by Pfizer in 2009, the Justice Department said.
Apr 27, 2016 at 12:36 | Source: PTI
Aurobindo Pharma today said it has received final approval from the US health regulator tomanufacture and market generic version of heartburn relief medicine Famotidine tablets.