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    Company profile for Zenara Pharma

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    Zenara`s Generics Nitazoxanide Receives Approval in US

    03 Feb 2025

    // FDA

    Zenara Pharma`s Generics Tafamidis Receives Tentative Approval in US

    21 Aug 2024

    // FDA

    Zenara's Generics Valsartan Receives Approval in US

    05 Aug 2024

    // FDA

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    About

    Our state-of-the-art manufacturing facility at Cherlapally, Hyderabad is designed, equipped and maintained as per latest cGMP norms. The company’s manufacturing facility is fully equipped to manufacture both Solid Orals (Tablets, Capsules) and Oral liquids in various therapeutic categories. Zenara has in-house capability to ensure regulatory compliance in all the markets we operate in. We are constantly strengthening our global supply chain with customers in key markets including United States of America, Europe, Australia, New Zealand, Canada, Far East Asia, GCC (Gulf Cooperation Council), Brazil among others.

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    Plot No.83/B, 84 & 87 to 96, Phase - III, IDA Cherlapally, Hyderabad - 500 051
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    +91 4027260848
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    info@biophore.com
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    https://www.zenarapharma.com/
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    Zenara`s Generics Nitazoxanide Receives Approval in US
    Zenara`s Generics Nitazoxanide Receives Approval in US

    03 Feb 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=214844

    FDA
    03 Feb 2025
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    Zenara Pharma`s Generics Tafamidis Receives Tentative Approval in US
    Zenara Pharma`s Generics Tafamidis Receives Tentative Approval in US

    21 Aug 2024

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218205

    FDA
    21 Aug 2024
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    Zenara's Generics Valsartan Receives Approval in US
    Zenara's Generics Valsartan Receives Approval in US

    05 Aug 2024

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218169

    FDA
    05 Aug 2024
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    Biophore, its subsidiary Zenara, receive first approval for Cannabidiol in India
    Biophore, its subsidiary Zenara, receive first approval for Cannabidiol in India

    15 May 2023

    // HEALTH ET

    https://health.economictimes.indiatimes.com/news/pharma/drug-approvals-launches/biophore-its-subsidiary-zenara-pharma-receive-first-approval-for-cannabidiol-in-india/100251790

    HEALTH ET
    15 May 2023
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    Zenara Pharma Generic Eliglustat Tartrate Receives Approval in the U.S
    Zenara Pharma Generic Eliglustat Tartrate Receives Approval in the U.S

    02 May 2023

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=212420

    FDA
    02 May 2023
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    Zenara's Generic Ertugliflozin Receives Approval in the U.S.
    Zenara's Generic Ertugliflozin Receives Approval in the U.S.

    04 Apr 2023

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=216842

    FDA
    04 Apr 2023
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    Zenara Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : BREXPIPRAZOLE

    Dosage Strength : 0.25MG

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    Application Number : 213477

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    Dosage Form : TABLET;ORAL

    Brand Name : BREXPIPRAZOLE

    Dosage Strength : 1MG

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    Approval Date :

    Application Number : 213477

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    Dosage Form : TABLET;ORAL

    Brand Name : BREXPIPRAZOLE

    Dosage Strength : 3MG

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    Approval Date :

    Application Number : 213477

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    BREXPIPRAZOLE

    Zenara Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : BREXPIPRAZOLE

    Dosage Strength : 0.5MG

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    Approval Date :

    Application Number : 213477

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    Regulatory Info :

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    BREXPIPRAZOLE

    Zenara Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : BREXPIPRAZOLE

    Dosage Strength : 2MG

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    Approval Date :

    Application Number : 213477

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    Regulatory Info :

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    Zenara Pharma

    Dosage Form : TABLET;ORAL

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    Dosage Strength : 4MG

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    Application Number : 213477

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    Brand Name : NITAZOXANIDE

    India
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    Regulatory Info : RX

    Registration Country : USA

    NITAZOXANIDE

    Zenara Pharma

    Dosage Form : TABLET;ORAL

    Brand Name : NITAZOXANIDE

    Dosage Strength : 500MG

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    Approval Date : 2025-02-03

    Application Number : 214844

    Regulatory Info : RX

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