US FDA inspects Vishakhapatnam facility of Solara Active PharmaThe US Food and Drug Administration (FDA) completes inspection of Solara Active Pharma Sciences' API manufacturing facility in Visakhapatna...
20 May, 2024, 12.12 PM IST
IOL Chemicals gets EDQM certification for API supply to EuropeThe European Directorate for the Quality of Medicines & HealthCare (EDQM) is a mandatory certification for distribution of any API/ pharma ...
07 Nov, 2022, 08.08 PM IST
GSK to recall Ranitidine from India after regulator alertBritish drugmaker will suspend release, distribution and supply of the heartburn drug.
26 Sep, 2019, 08.20 AM IST
Lupin gets EDQM nod for its Mandideep facilityThe inspection was focused on the application for certificate of suitability for the dossier of Cefaclor along with facility inspection for...
30 Jul, 2018, 02.30 PM IST
Will call FDA for re audit once consultants are confident for reinspect: Adhish Patil of Aarti DrugsThe thing is business things are looking good, in fact, the export market has started looking good in the second quarter so we hope that it...
26 Sep, 2016, 03.41 PM IST
Anuh Pharma recovers 14% from day's low on suspended drugs clarification“The company does not expect significant effect on its top & bottom line since the company have very good presence in Indian and rest of wo...
16 Mar, 2016, 10.20 AM IST
European drug regulator suspends Anuh Pharma's three drugsFollowing the inspection of it's manufacturing site, European Directorate for the Quality of Medicines and Healthcare has suspended certifi...
15 Mar, 2016, 08.44 PM IST
Granules India shareholders approve Auctus acquisitionGranules India, a city-based pharmaceutical manufacturer, said its shareholders have approved proposed acquisition of Auctus Pharma.
07 Dec, 2013, 06.26 PM IST
USFDA pulls up Smruthi Organics for norms violation in unitSmruthi Organics today said it has received a notification from the USFDA highlighting violations of manufacturing norms at its Solapur pla...
21 Oct, 2013, 02.49 PM IST
- Elder Pharma set to enter regulated markets of European Union
Diosmin, a semi-synthetic drug, is an oral phlebotropic drug used in the treatment of venous system related diseases. Disease (HD), Microci...
25 Nov, 2012, 10.54 AM IST
- Elder Pharma's Q2 profit jumps 22 pc to Rs 24 crore
Elder Pharma today said its consolidated net profit rose by 22 per cent to Rs 23.60 crore in the July-September quarter.
12 Nov, 2012, 06.35 PM IST
- Elder Pharmaceuticals gets suitability certificate from EDQM for Diosmin
Drug firm Elder Pharmaceuticals today said it has received certificate of suitability for 'Diosmin API', a drug used for the treatment of d...
06 Nov, 2012, 08.11 PM IST
- Aanjaneya Lifecare gets Rs 60 cr order for making cough syrup
Bulk drug maker said it has received orders worth Rs 60 cr from Wockhardt and Cipla, for manufacturing cough syrup 'Recodex'.
28 Jun, 2011, 05.49 PM IST
- IOLCP gets nod for facilities from European health regulator
Drug firm IOL Chemicals and Pharmaceuticals said it has received the certificate of suitability from European health regulator for its manu...
09 Nov, 2010, 12.53 PM IST
- Unichem gets EU nod for drug to treat enlarged prostate
Unichem Laboratories on Thursday said it has received a certificate of suitability for its generic drug for treatment of enlarged prostate ...
23 Sep, 2010, 08.49 PM IST
- CARE assigns IPO Grade 2 to Parabolic Drugs
CARE has assigned 'CARE IPO Grade 2' to the Rs 200 crore initial public offer of Parabolic Drugs Ltd, indicating 'Below Average Fundamental...
03 Jun, 2010, 11.57 AM IST
- Marksans Pharma gets European approval
Marksans Pharma gets the approval to market its Ciprofloxacin Hydrochloride drug substance in Europe.
26 Sep, 2007, 07.20 PM IST