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    Company profile for Navinta

    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    Expand your portfolio with Egis- value-added generics, API capabilities, and reliable contract services to drive your growth.

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    About

    Navinta, LLC is a privately held generic pharmaceutical company, established in 2003, dedicated to the development and commercialization of pharmaceutical products to treat patients with chronic and life-threatening diseases. Navinta means “novelty” inspiring a culture of transforming ideas into technology and advancing innovation to the marketplace with new medicines. Navinta has focused its research and regulatory activi...
    Navinta, LLC is a privately held generic pharmaceutical company, established in 2003, dedicated to the development and commercialization of pharmaceutical products to treat patients with chronic and life-threatening diseases. Navinta means “novelty” inspiring a culture of transforming ideas into technology and advancing innovation to the marketplace with new medicines. Navinta has focused its research and regulatory activities on developing new formulations, complex products, and unique pharmaceutical delivery systems. Navinta owns 21 process and product patents, 25 active Drug Master Files, and has 14 approved ANDA commercial products.

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    NavintaUnited_States_of_America Flag
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    Country
    U.S.A
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    Address
    1499 Lower Ferry Road Ewing, NJ 08618
    Telephone
    Telephone
    +1 609.883.1135
    Client Email
    Email
    enquiries@pharmacompass.com
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    Website
    https://www.navinta.com/
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    NEWS #PharmaBuzz

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    Everstone Invests $270M In Apothecon-Navinta Pharma Platform
    Everstone Invests $270M In Apothecon-Navinta Pharma Platform

    14 Apr 2026

    // BUSINESS STD

    https://www.business-standard.com/companies/news/everstone-capital-invests-270-million-in-apothecon-navinta-platform-126041400588_1.html

    BUSINESS STD
    14 Apr 2026
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    Navinta’s Generics Sodium Phenylbutyrate Receives Approval in US
    Navinta’s Generics Sodium Phenylbutyrate Receives Approval in US

    17 Feb 2026

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=220418

    FDA
    17 Feb 2026
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    Navinta’s Generics Diazepam Receives Approval in US
    Navinta’s Generics Diazepam Receives Approval in US

    14 Nov 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=217468

    FDA
    14 Nov 2025
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    Navinta’s Receives First Generic Approval for Diazepam in US
    Navinta’s Receives First Generic Approval for Diazepam in US

    14 Nov 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&varApplNo=217468

    FDA
    14 Nov 2025
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    Navinta’s Generics Sevelamer Carbonate Receives Approval in US
    Navinta’s Generics Sevelamer Carbonate Receives Approval in US

    27 Oct 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=219931

    FDA
    27 Oct 2025
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    Navinta’s Generics Nicardipine Hydrochloride Approved in US
    Navinta’s Generics Nicardipine Hydrochloride Approved in US

    25 Jun 2025

    // FDA

    https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218638

    FDA
    25 Jun 2025
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    Navinta is a supplier offers 9 products (APIs, Excipients or Intermediates).

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.

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