loader
Please Wait
Applying Filters...

Seqens Seqens

X
menu

    Market Place

    Market Place

    Post Enquiry

    Post Enquiry
    menu

    List of Drug Master Files (DMF) for 25342 Active Pharmaceutical Ingredient (API) submitted to the U.S. FDA. Original Data : FDA Website

    Client Virtual Booth
    Menu

    Chemport Inc

    EVENTS

    • Webinars & Exhibitions

    PRESENTATION(s)

    VIDEO(s)

    DIGITAL CONTENT

    APIs // Active Pharmaceutical Ingredients

    DEVELOPMENTS

    PharmaCompass

    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

    Left Arrow
    Right Arrow
    Filters Filter
    Cross PopUp
    FILTER :

    filter

    01 Chemport Inc (1)

    filter

    01 OMEGA-3-ACID ETHYL ESTERS (1)

    filter

    01 United Kingdom (1)

    filter

    01 Active (1)

    filter

    01 Complete (1)

    ListList of Suppliers
    refresh Reset Filter
    refresh Reset Filter
    product-page Supplier Virtual Booth
    price-trend Ask Us

    CHEMPORT INC

    Contact Supplier
      Virtual Booth Upload your Marketing & Sales content on your company Virtual Booth, click HERE
      Post an Enquiry Post an Enquiry
      Flag United Kingdom
      Virtual Booth Virtual Booth
      Digital Content Digital Content

      OMEGA-3-ACID ETHYL ESTERS

      PDF Supplier PDF
      URL Supplier Web Content
      25342
      Active
      2011-09-07
      Complete
      2014-04-28
      2013-11-06
      II
      ASK
      US
      PHARMACOMPASS
      Upload
      your Marketing & Sales content

      Looking for Drug Master Files (DMF) for 25342 of Chemport Inc

      Looking for Drug Master Files (DMF) for 25342 of Chemport Inc 1

      20

      Chemport Inc, based in United Kingdom, is a pharmaceutical company.

      One of their notable products is OMEGA-3-ACID ETHYL ESTERS, with a corresponding US DMF Number 25342.

      Remarkably, this DMF maintains an Active status since its submission on September 07, 2011, highlighting commitment to regulatory compliance.

      Their GDUFA DMF Review was successfully complete, with a review date of April 28, 2014, and payment made on November 06, 2013, indicating their dedication to facilitating drug approvals, Categorized as Type II

      Post Enquiry
      POST ENQUIRY