Pharma News

Rockwell Industries ties with DRL for freezer to store Sputnik V

Rockwell Industries ties with DRL for freezer to store Sputnik V

Rockwell Industries, a cold chain appliance manufa

Pfizer jab endorsed for kids, yet first others should be vaccinated

Pfizer jab endorsed for kids, yet first others should be vaccinated

Moderna and Pfizer have released data suggesting t

Pharma News

Rockwell Industries ties with DRL for freezer to store Sputnik V

Rockwell Industries, a cold chain appliance manufacturer on Wednesday announced its strategic partnership with Dr Reddy’s Labs, to provide its World Health Organisation – Performance, Quality and Safety certified Covid-19 vaccine freezersto enablestorage of Sputnik V vaccine in India. According to a release by Rockwell, the vaccine freezer plays a very critical role in the safety

Pfizer jab endorsed for kids, yet first others should be vaccinated

Moderna and Pfizer have released data suggesting that their vaccines are well tolerated in adolescents and highly effective in preventing COVID-19. Canada, the US and the EU have already authorised the Pfizer vaccine in children as young as 12. And the UK has just approved the use of the Pfizer vaccine in children aged 12

Glenmark Pharma gets last gesture from USFDA for Theophylline ER tablets

Glenmark Pharma on Friday said it has received final approval from the US health regulator for Theophylline extended-release (ER) tablets. Theophylline extended-release tablets are used to prevent and treat wheezing, shortness of breath, and chest tightness caused by asthma, chronic bronchitis, emphysema, and other lung diseases. In a regulatory filing Glenmark Pharmaceuticals said it has

Moderna looks for full FDA endorsement for its COVID-19 vaccine

American pharmaceutical company Moderna says it has begun the process to win full U.S. regulatory approval for the use of its COVID-19 vaccine in adults. Moderna announced on Tuesday it has begun a “rolling submission” to the Food and Drug Administration of data from its studies of the two-dose vaccine. Moderna’s vaccine already has been

Bajaj Healthcare launches drug to treat black fungus infection in COVID-19 patients

Bajaj Healthcare on Friday launched Posaconazole API, used in treating Mucormycosis (black fungus) infection in COVID-19 patients. The company has received approval from FDA (Food and Drugs Administration) Gandhi Nagar, Gujarat (India), to manufacture and market Posaconazole API as approved medication for treating Mucormycosis in India, Bajaj Healthcare said in a regulatory filing. Bajaj Healthcare

Glenmark Pharma gets USFDA gesture for Icatibant Injection

Drug major Glenmark Pharma on Monday said it has received final approval from the US health regulator for Icatibant Injection, indicated for the treatment of acute attacks of hereditary angioedema (HAE). Hereditary angioedema (HAE) is a disorder that results in recurrent attacks of severe swelling. The approved product is a generic version of Firazyr Injection

Bal Pharma dispatches antiviral drug Favipiravir at Rs 85/tablet

Drug maker Bal Pharma on Monday said it has launched antiviral drug Favipiravir in the domestic market under the brand name BALflu for the treatment of COVID-19. The Bengaluru-based company said its formulation would be available in tablet form with 400 mg strength. Favipiravir is being used for patients with mild to moderate COVID-19 infection as it

Sun Pharma reviews 50,868 bottles of diabetes drug in US

New Delhi, May 21 (PTI) Drug major Sun Pharma is recalling 50,868 bottles of diabetes drug Metformin HCl extended-release tablets in the US market, according to the US Food and Drug Administration (USFDA). The US-based arm of the drug firm is recalling the affected lot of 500 mg tablets (in 500 count bottles) due to

Natco Pharma gets USFDA gesture for generic cancer trearment drug

New Delhi, May 22 (PTI) Natco Pharma on Saturday said it has received approval from the US health regulator for generic Lenalidomide capsules indicated for treatment of adults with multiple myeloma, mantle cell lymphoma and myelodysplastic syndromes. The company has received final approval from the US Food and Drug Administration (USFDA) for its abbreviated new