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    • Laurus Labs gets USFDA...

    Laurus Labs gets USFDA nod to Hydroxychloroquine tablets for treating malaria

    Farhat NasimWritten by Farhat Nasim Published On 2019-03-12T12:01:23+05:30  |  Updated On 17 Aug 2021 12:55 PM IST

    Hydroxychloroquine tablet is also used, usually with other medications, to treat certain auto-immune diseases (lupus, rheumatoid arthritis) when other medications have not worked or cannot be used.


    New Delhi: Hyderabad-based, Laurus Labs gets final approval from the US health regulator for its Hydroxychloroquine tablets for treating malaria, the company has also received a tentative approval for an abbreviated new drug application (ANDA) for Abacavir, Dolutegravir, and Lamivudine, tablets 600 mg/50 mg/300 mg.


    The company has received final approval from the United States Food and Drug Administration (USFDA) for Hydroxychloroquine tablets in the strength of 200 mg, Laurus Labs said in a filing to the BSE. Hydroxychloroquine tablets are used for treatment of malaria and certain autoimmune diseases.


    Hydroxychloroquine is used to prevent or treat malaria infections caused by mosquito bites. It does not work against certain types of malaria (chloroquine-resistant). This medication is also used, usually with other medications, to treat certain auto-immune diseases (lupus, rheumatoid arthritis) when other medications have not worked or cannot be used. It belongs to a class of medications known as disease-modifying antirheumatic drugs (DMARDs).


    The product is generic version of Concordia Pharmaceuticals Inc's Plaquenil tablets in the same strength, it added.


    Also Read:Laurus Labs gets tentative USFDA approval for HIV combo drug


    Hydroxychloroquine tablets are used for treatment of certain type of malaria. It is also used, usually with other medications, to treat certain autoimmune diseases (lupus, rheumatoid arthritis) when other medications have not worked or cannot be used, Laurus Labs said.


    "The company has also received a tentative approval for an abbreviated new drug application (ANDA) for Abacavir, Dolutegravir, and Lamivudine, tablets 600 mg/50 mg/300 mg from USFDA," it added.

    The products will be commercialised from the company's manufacturing site located at Atchutapuram in Visakhapatnam, the company said.

    The Company is one of the manufacturers of Active Pharmaceutical Ingredients (APIs) for anti-retroviral (ARV) and Hepatitis C. Laurus also manufactures APIs in Oncology and other therapeutic areas. Laurus Labs also forayed into Finished Dosages Forms capabilities on the back of existing strengths in APIs.


    Also Read: Laurus Labs gets USFDA approval for diabetes drug

    AbacavirANDAautoimmuneConcordiaConcordia Universitydengu medicineDolutegravirgenerichealthhealth carehydroxychloroquineLamivudineLaurusLaurus Labsmalariamalaria medicinemedicalmedicinepharma newsPlaquenilUSFDA
    Source : with inputs

    Disclaimer: This site is primarily intended for healthcare professionals. Any content/information on this website does not replace the advice of medical and/or health professionals and should not be construed as medical/diagnostic advice/endorsement or prescription. Use of this site is subject to our terms of use, privacy policy, advertisement policy. © 2020 Minerva Medical Treatment Pvt Ltd

    Farhat Nasim
    Farhat Nasim

      Farhat Nasim joined Medical Dialogue an Editor for the Business Section in 2017. She Covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She is a graduate of St.Xavier’s College Ranchi. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751 To know about our editorial team click here

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