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AstraZeneca Receive US FDA Approval for its Lung Cancer Drugs

The US Food and Drug Administration (FDA) approved AstraZeneca’s cancer drugs Imfinzi and Imjudo in combination with chemotherapy to treat patients with stage 4 non-small cell lung cancer. This approval is based on the phase 3 data published in September 2021. Imfinzi and Imjudo with chemotherapy have shown an overall 23

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US FDA Approves Generic Hypertension Drug of Zydus Lifesciences

The US Food and Drug Administration (FDA) has approved Zydus Lifesciences’ hypertension drugs Bisoprolol Fumrate and Hydrochlorothiazide tablets in the United States. The US FDA has given clearance to Zydus Lifesciences to market generic medicines in the United States in multiple strengths. With increasing cases of hypertension, the combination of Bisoprolol

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The a2 Milk Company Receive FDA Discretion to Supply Infant Milk Formula in the US

New Zealand’s The a2 Milk Company has received enforcement discretion from the US Food and Drug Administration to supply its a2 Platinum Premium Infant Milk Formula to the US market to help overcome the ongoing supply crisis. a2 Platinum is a leading international infant milk formula brand. The a2 Platinum is

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US FDA Approves Gilead Sciences Inc.’s Vemlidy to Treat Chronic Hepatitis B in Pediatric Patients

The US Food and Drug Administration (FDA) has approved the supplemental new drug application (sNDA) for Vemlidy (tenofivir alafenamide) 25 mg tablets by Gilead Sciences, Inc., to treat chronic hepatitis B virus (HBV) in pediatric patients older than 12 years with compensated liver disease. Vemlidy is a targeted, novel prodrug of

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US FDA Approved Johnson & Johnson’s Blood Cancer Therapy

The US Food and Drug Administration (FDA) has approved Johnson & Johnson’s new therapy to treat a type of multiple myeloma, and the therapy has given another option of treatment to patients suffering with incurable blood cancer. According to Johnson & Johnson, teclistamab therapy, which is branded as Tecvayli, is approved

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US FDA Approved Zhiyi Biotech’s SK10 to Treat Chemotherapy-induced Diarrhea

Zhiyi Biotech has announced that the US Food and Drug Administration (FDA) has approved the Investigational New Drug (IND) application of the company to develop SK10 (Inactivated Bacteroids fragilis) for the treatment of Chemotherapy-induced Diarrhea (CID). The approval of the IND application authorizes Zhiyi Biotech to conduct a Phase 1

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US FDA Authorized World’s First Plant-Based Medical Grade Face Mask

The US Food and Drug Administration (FDA) has authorized PADM Medical PRECISION ECO plant-based procedural mask with earloops under emergency use authorization (EUA). The face mask is the first plant based procedural mask in the world to receive EUA for use in medical and healthcare industries. PADM Medical Group of Companies,

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