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    Tag: anda

    You Searched For "anda"
    USFDA Caution: Lupin gets OAI letter for MP plant

    USFDA Caution: Lupin gets OAI letter for MP plant

    Medical Dialogues Bureau17 March 2019 9:45 AM IST
    Lupin has received a letter from the US Food and Drug Administration (USFDA) classifying the inspection conducted at its Mandideep (Unit 1) facility...
    Glenmark gets USFDA nod for generic version of acne treatment gel

    Glenmark gets USFDA nod for generic version of acne treatment gel

    Farhat Nasim17 March 2019 9:21 AM IST
    New Delhi: Glenmark Pharmaceuticals Friday said it has received final approval from the US health regulator for its generic version of BenzaClin gel...
    Laurus Labs gets USFDA nod to Hydroxychloroquine tablets for treating malaria

    Laurus Labs gets USFDA nod to Hydroxychloroquine tablets for treating malaria

    Farhat Nasim12 March 2019 12:01 PM IST
    Hydroxychloroquine tablet is also used, usually with other medications, to treat certain auto-immune diseases (lupus, rheumatoid arthritis) when other...
    Alembic Pharma JV Aleor gets USFDA nod for Clobetasol Propionate ointment

    Alembic Pharma JV Aleor gets USFDA nod for Clobetasol Propionate ointment

    Farhat Nasim6 March 2019 9:45 AM IST
    The company's JV, Aleor Dermaceuticals Ltd, has received approval from the US Food and Drug Administration (USFDA) for its abbreviated new drug...
    Shilpa Medicare gets USFDA nod for Gemcitabine to treat types of cancer

    Shilpa Medicare gets USFDA nod for Gemcitabine to treat types of cancer

    Farhat Nasim27 Feb 2019 9:30 AM IST
    The company has received US Food and Drug Administration (USFDA) approval for its Abbreviated New Drug Application (ANDA), Gemcitabine for injection...
    Alembic Pharma gets USFDA nod for Acetazolamide extended release capsules

    Alembic Pharma gets USFDA nod for Acetazolamide extended release capsules

    Farhat Nasim21 Feb 2019 9:45 AM IST
    Acetazolamide extended-release capsule is therapeutically equivalent to the reference listed drug, Diamox Sequels, 500 mg, of Teva Branded...
    Alembic Pharma gets USFDA nod for Olopatadine Hydrochloride ophthalmic solution

    Alembic Pharma gets USFDA nod for Olopatadine Hydrochloride ophthalmic solution

    Farhat Nasim17 Feb 2019 9:30 AM IST
    The company has received approval from the US Food and Drug Administration (USFDA) for its abbreviated new drug application (ANDA) Olopatadine...
    Alembic Pharma gets USFDA nod for Olopatadine Hydrochloride ophthalmic solution

    Alembic Pharma gets USFDA nod for Olopatadine Hydrochloride ophthalmic solution

    Medical Dialogues Bureau10 Dec 2018 9:15 AM IST
    New Delhi: Drug firm Alembic Pharma on Monday said it has received approval from the US health regulator for Olopatadine Hydrochloride ophthalmic...
    Mankind Pharma eyes 1 billion Dollar Turnover by 2021: Chairman RC Juneja

    Mankind Pharma eyes 1 billion Dollar Turnover by 2021: Chairman RC Juneja

    Medical Dialogues Bureau2 Oct 2018 11:43 AM IST
    New Delhi: Drugmaker Mankind Pharma is looking at achieving a turnover of USD 1 billion by 2021 from the present Rs 5,200 crore, a top company...
    Cipla gets USFDA nod for generic version of Renvela tablets

    Cipla gets USFDA nod for generic version of Renvela tablets

    supriya kashyap kashyap28 Oct 2017 9:18 AM IST
    New Delhi: Drug major Cipla said its subsidiary InvaGen Pharmaceuticals Inc has received final approval from the US health regulator for Sevelamer...
    Ajanta Pharma gets USFDA nod for Aripiprazole Tablets

    Ajanta Pharma gets USFDA nod for Aripiprazole Tablets

    savita thakur thakur15 Sept 2016 12:33 PM IST
    Ajanta Pharma Limited announces the receipt of final approval for Aripiprazole Tablets (2mg, 5mg, 10mg, 15mg, 20mg, 30mg), the bio equivalent generic...
    Glenmark gets USFDA nod for contraceptive tablets

    Glenmark gets USFDA nod for contraceptive tablets

    savita thakur thakur25 Feb 2016 1:13 PM IST
    New Delhi: Glenmark Pharmaceuticals has received the final nod from the US health regulator for generic oral contraceptive norgestimate ethinyl...
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