Under new terms, DRL to hold back Rs 300 crore and release it if the revenue from sale of the products forming part of the business undertaking during the 12 months post-closing exceeds Rs 480 cr
The USFDA has recently given an emergency approval to the drug for use on coronavirus patients
The company said, with this, all facilities under warning letter are now determined as Voluntary Action Indicated (VAI)
Local pharma units have already started work on developing patented drugs, some have already approached regulator for approvals
Patient groups urge govt to revoke Gilead's remedesivir patent in the wake of the crisis
It's the therapeutic generic equivalent of Geodon Injections
Earlier, the drug major had said that the US health regulator has issued a Form 483 with two observations after inspecting the facility but later it was issued revised Form 483 with one observation
21,026 votes, which accounted for the rest 0.02 per cent, were posted against the resolution, it added
First Indian firm to get contract for supplying generic schizophrenia drug to public hospitals there
Earnings were driven by one-off gains
The company initiated a voluntary recall of 2,280 bottles of Atorvastatin Calcium 40 mg 500 tablets on August 2