Lupin gets USFDA nod to market its mania and epilepsy treatment drug in USThe company has received approval from the United States Food and Drug Administration (USFDA) for its Divalproex Sodium extended-release ta...
22 Oct, 2019, 05.31 PM IST
Taro drug pricing probe may widen to other generic drug makersResearch by IIFL shows several generic drug companies, including a few top Indian generic drug makers, effected steep price increases withi...
14 Sep, 2016, 09.03 AM IST
Dr Reddy's Laboratories recalls anti-seizure, hypertension drugs from US marketThe firm has started recalling Divalproex Sodium extended-release tablets as it has failed dissolution tests.
29 Jun, 2015, 01.02 PM IST
US legal authorities seek information on Dr Reddy's Laboratories drug pricing mechanismAttorney Generals of Texas and California have separately sought information on pricing of some drugs sold by Dr Reddy's Laboratories in th...
25 Feb, 2015, 11.18 AM IST
Aurobindo gets USFDA nod to market mental illness drugAccording to IMS sales data, the product had a market size of around USD 690 million for the twelve months ended March 2014.
03 Jun, 2014, 02.55 PM IST
Analysts see over 20% upside in Cadila Healthcare after strong Q3 showGiven the overall technical picture, there is a strong possibility of a price breakout occurring at the end of February 2014.
19 Feb, 2014, 04.50 PM IST
- Aurobindo Pharma gets USFDA approval for CNS drug
Aurobindo Pharma said it has received US health regulator's approval to manufacture and sell generic Divalproex Sodium Delayed-Release tabl...
25 Apr, 2011, 02.26 PM IST
- Unichem gets USFDA nod for Divalproex; stocks up
Unichem Laboratories has received approval from USFDA for Divalproex Sodium delayed release tablets USP 125mg, 250mg and 500mg.
07 Apr, 2011, 12.13 PM IST
- Orchid Chemicals gets USFDA approval for divalproex tablets
Orchid Chemicals & Pharmaceuticals has received US Food and Drug Administration approval for its abbreviated new drug application for dival...
04 Dec, 2008, 12.13 PM IST
- Sun Pharma gets approval form USFDA for Depakote Tablet
Sun Pharmaceutical has received tentative approval for the abbreviated new drug application--generic Depakote , divalproex sodium delayed r...
14 Feb, 2008, 06.33 PM IST
- Abbott files patent suit against Zydus Cadila in US court
US-based Abbott Laboratories seeks to stop the Indian company, Zydus Cadila, from selling generic version of its drug, Depakote, in the US.
11 Dec, 2007, 12.04 AM IST
- Cadila bags USFDA nod for 3 products
Pharmaceutical firm, Cadila Healthcare today said USFDA has given its nod it for the company's three products, taking the group's total num...
19 Mar, 2007, 03.20 PM IST
- New drug dose helps local firms regain health in US
Domestic pharma majors are witnessing sharp recovery in their US business.
21 Aug, 2006, 12.56 AM IST
- Wockhardt gets nod for new drug
Wockhardt Ltd has received tentative approval from the USFDA for anti-epileptic drug, Divalproex Sodium delayed-release tablets.
14 Jun, 2006, 02.40 PM IST