Deal would help Wockhardt focus on international operations, novel pipeline R&D
Firm takes a Rs 1,110 crore hit with generic versions of its Nuvaring drug hitting the market; financial results run completely contra to analyst expectations
In the first 11 trading days of the current calendar year, Dr Reddy's has outperformed the market by surging 6 per cent on expectations of earnings improvement.
Lupin, Sun Pharmaceutical, Cadila Healthcare, Aarti Drugs and Aurobindo Pharma were up in the range of 2 per cent to 3 per cent.
21,026 votes, which accounted for the rest 0.02 per cent, were posted against the resolution, it added
Firm has outperformed domestic pharma market in 7 of last 8 quarters
Amneal's EluRyng is the first generic version of this low competition drug, which the company plans to launch this month
Bortezomib is an active ingredient similar to that of the once blockbuster cancer treatment Velcade of Millennium Pharmaceuticals
Analysts at SBICAP Securities upgraded the stock with 'buy' rating and target price of Rs 3,200 per share
The products are manufactured either in the plant owned by KRRP in China, or partners in China, or in India by Dr. Reddy's
Dr Reddy's was in the news for falling short of expectations during routine audits conducted by the US drug regulator
According to Prasad, the relevance of Indian pharma sector as a provider of affordable alternative to the world remains intact
Dr Reddy's 'Celevida' is formulated to have high protein, high fibre and slowly digested carbohydrates
An amount of Rs 17 crore is recognised as a possible refund liability (as a reduction from revenue) arising out of the company's decision to recall the said product
The drug major has reported a 26% increase in revenues at Rs 4,801 crore for Q2
Better top-lines numbers come in despite a flattish growth in the firm's US business.
Ranitidine sales account for 2 per cent of Strides sales and 6 per cent of its profit after tax
Drug major Dr Reddy's on Saturday said it has received four observations from the US health regulator USFDA for its facility at Srikakulam in Andhra Pradesh. The audit of the company's API Srikakulam Plant (SEZ) by the United States Food and Drug Administration (USFDA) was completed on Friday, the Hyderabad-based pharma major said in a regulatory filing. Dr Reddy's further said that it would address the four concerns within the stipulated timeline. "The audit of our API Srikakulam Plant (SEZ), Andhra Pradesh, by the USFDA, has been completed on October 25, 2019. We have been issued a Form 483 with four observations," said Dr Reddy's. It further said: "We will address them comprehensively within the stipulated timeline." As per the US health regulator, "an FDA Form 483 is issued to firm management at the conclusion of an inspection when an investigator(s) has observed any conditions that in their judgment may constitute violations of the Food Drug and Cosmetic (FD&C) Act and ...
First Indian firm to get contract for supplying generic schizophrenia drug to public hospitals there
First Indian firm to get contract for supplying generic schizophrenia drug to public hospitals there