Marksans Pharma gets US FDA nod for Esomeprazole Magnesium DR Capsules USP, 20 mg (OTC) EP News Bureau Oct 3, 2023 Esomeprazole is used to treat certain stomach and esophagus problems such as acid reflux and ulcer
Marksans receives USFDA approval for Guaifenesin ER Tablets (OTC) EP News Bureau Aug 22, 2023 Guaifenesin extended-release tablets help to loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways…
Marksans Pharma raises Rs 372.40 crore in equity via conversion of warrants issued to OrbiMed and… EP News Bureau Jan 20, 2023 The warrants are converted at a price of Rs 74 per share, reflecting the promoter's and OrbiMed's commitment to the company
Marksans Pharma reports financial results for Q2 and H1FYF23 EP News Bureau Nov 15, 2022 Operating revenue at Rs 452.6 crore, increased 25.5 per cent YoY, driven by a growth in the existing products as well as market…
World Economic Forum recognises Dr Reddy’s Hyderabad factory as part of its Global Lighthouse… EP News Bureau Oct 12, 2022 With this recognition, the facility joins the GLN, a community of over 100 manufacturers that are showing leadership in applying…
Marksans acquires capacity from Tevapharm India EP News Bureau Oct 12, 2022 The transaction is in cash consideration, and is expected to be finalised by 1st April, 2023, subject to the usual closing…
Marksans Pharma gets UK MHRA nod for diarrhoea medication Press Trust of India Dec 11, 2021 The capsules will be manufactured at the company's Goa-based oral dosage facility
Marksans Pharma and Sun Pharma voluntarily recall metformin EP News Bureau Oct 6, 2020 oth the companies are recalling metformin because it may contain N-nitrosodimethylamine (NDMA) above the acceptable intake limit.
Marksans Pharma expands recalls of metformin hydrochloride tablets EP News Bureau Oct 4, 2020 It is due to NDMA content in some lots that exceed the acceptable daily intake limit of 96ng/day
Marksans Pharma appoints Dr Meena Rani Surana as Independent Woman Director EP News Bureau Sep 5, 2020 She has about 27 years of experience in pharmaceutical regulatory affairs, quality assurance, formulation and pre-formulation