As per the latest Enforcement Report of US Food and Drug Administration (USFDA), Aurobindo Pharma USA Inc, a subsidiary of Hyderabad-based drug maker, is recalling over 1 lakh bottles of Cinacalcet tablets in multiple strengths.
The company reported a consolidated loss after tax of Rs 180.3 crore in the same quarter last fiscal, Glenmark Pharmaceuticals said in a regulatory filing
The domestic formulations market is estimated to be at Rs 2 lakh crore, with a growth rate of 11 percent over the past two decades
Glenmark Q4: Revenue rose two percent from the previous year to Rs 3,063 crore, from Rs 3,000.5 crore in the same period a year ago
Glenmark Specialty SA, a unit of Mumbai-based drug maker, has inked exclusive marketing and distribution agreement with BeiGene.
The final approval by the US Food & Drug Administration (USFDA) is for brimonidine tartrate and timolol maleate ophthalmic solution of strength 0.2 per cent/0.5 per cent, Glenmark said in a statement.
As per the latest Enforcement Report by the US Food and Drug Administration (USFDA), Lupin is recalling 26,352 bottles of Rifampin Capsules (300 mg), an antibiotic medication in the US market.
Lupin recalled 26,352 bottles of Rifampin capsules, used in the treatment of tuberculosis
The opening date (commencement of the tendering period) for the open offer has been fixed on February 15, 2024, and will close on February 29, 2024, as per the letter of offer, the letter said.
Glenmark Pharmaceuticals recalled 37,200 bottles of Indomethacin capsules and Sun Pharma recalled 2016 bottles of buPROPion Hydrochloride Extended-Release Tablets.
In its latest enforcement report, the US health regulator said Princeton-based Dr Reddy’s Laboratories, Inc., a unit of the Hyderabad-based drug firm, is recalling 1,656 bottles of Montelukast sodium tablets.
Glenmark Pharma had undergone a similar exercise in May 2019, when it spun off its API business into a new entity called Glenmark Life Sciences, which made its public market debut in August 2021