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    NEWS

    DRUGS & DEVELOPMENTS

    MARKET INTEL by PharmaCompass

    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

    Enforcement Report - Week of July 24, 2024

    FDA

    AM Regent`s Generic Dextrose Receives Approval in US

    FDA

    Enforcement Report - Week of January 10, 2024

    FDA

    Health Canada Issues Recall of Baxter`s 5% Dextrose Injection, USP: Solution bags may be leaking in affected lots

    HEALTH CANADA

    Enforcement Report - Week of September 6, 2023

    FDA

    Enforcement Report - Week of August 9, 2023

    FDA

    Enforcement Report - Week of May 31, 2023

    FDA

    Health Canda Issues Recall of ICU Medical Canada`s Dextrose 50 mg/mL Injection USP

    HEALTH CANADA

    Enforcement Report - Week of May 24, 2023

    FDA

    Health Canda Issues Recall of B. Braun Medical`s Heparin sodium in 5% Dextrose injection

    HEALTH CANADA

    Enforcement Report - Week of February 22, 2023

    FDA

    SterRx, LLC Issues Voluntary Nationwide Recall of Sodium Bicarbonate in 5% Dextrose Injection 150mEq per 1,000 mL

    FDA

    B. Braun Medical Issues Voluntary Nationwide Recall of One (1) Lot of Ceftazidime for Injection USP and Dextrose Injection USP

    FDA

    AuroMedics Pharma Issues Voluntary Nationwide Recall of Levofloxacin in 5% Dextrose 250mg/50mL

    FDA

    Health Canada Issues Recall of Baxter Corporation`s Dianeal PD4 CAPD

    FDA

    Health Canada Issues Recall of Pfizer Canada ULC LMD 10% IN DEXTROSE 5%

    HEALTH CANADA

    Enforcement Report - Week of July 25, 2018

    FDA

    Enforcement Report - Week of May 9, 2018

    FDA

    AuroMedics Pharma LLC Issues Voluntary Nationwide Recall of Levofloxacin in 5% Dextrose 250mg/50mL

    FDA

    PharMEDium Services, LLC Issues Voluntary Nationwide Recall of all unexpired lots of Oxytocin Compounded with Lactated Ringers or Lactated Ringers & Dextrose

    FDA

    Enforcement Report - Week of July 19, 2017

    FDA

    Hospira Issues a Voluntary Nationwide Recall For One Lot Of 25% Dextrose Injection, USP (Infant) Due To The Presence of Particulate Matter

    FDA

    Enforcement Report - Week of April 12, 2017

    FDA

    Enforcement Report - Week of April 5, 2017

    FDA

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