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    Zydus Cadila

    Zydus Cadila gets conditional gesture from USFDA to showcase type-2 diabetes drug

    Zydus Cadila on Saturday said it has gotten conditional gesture from the US wellbeing controller to showcase conventional Empagliflozin and Metformin Hydrochloride tablets, utilized for the board of type-2 diabetes, in the American market. The organization has gotten speculative endorsement from the United States Food and Drug Administration (USFDA) to advertise Empagliflozin and Metformin Hydrochloride

    Cadila Healthcare increases after conditional USFDA endorsement for diabetes medicate

    Cadila Healthcare bounced 2.48% to Rs 332 after the organization said it got speculative endorsement from the US tranquilize controller for Empagliflozin and Metformin Hydrochloride tablets. The organization has gotten conditional endorsement from the US Food and Drug Administration (USFDA) to showcase Empagliflozin and Metformin Hydrochloride tablets, 5 mg/500 mg, 5 mg/1000 mg, 12.5 mg/500

    Zydus Cadila looks for endorsement to utilize hepatitis medicate for Covid-19 clinical preliminaries

    The nation’s top medication controller, Drug Controller General of India (DCGI), has gotten an application from Zydus Cadila, the leading worldwide pharmaceutical organization in India, to direct clinical preliminary utilizing antiviral medication ‘Pegylated Interferon Alpha-2b’ in grown-up Covid-19 patients. So far in India, the Pegylated Interferon Alpha-2b medication has been utilized for the treatment of

    Zydus Cadila dispatches COVID-19 medication Remdesivir in India

    Drug firm Zydus Cadila on August 13 stated it has established Remdesivir under the brand name Remdac, used to treat patients experiencing severe signs of COVID-19, in the Indian market. Priced at Rs 2,800 per 100 mg vial, Remdac is the most economical Remdesivir brand in India, Zydus Cadila said in a regulatory filing. The

    Zydus Cadila gets speculative USFDA gesture for generic drug

    New Delhi, Oct 19 Drug firm Zydus Cadila on Monday said it has received tentative approval from the US health regulator to advertise Tofacitinib extended-release pills, used to treat ulcerative colitis, in the American market. The company has received tentative approval from the US Food and Drug Administration (USFDA) for the item which is the