NetFind Web Search

  1. Ads

    related to: generic application form

Search results

  1. Results From The WOW.Com Content Network
  2. Abbreviated New Drug Application - Wikipedia

    en.wikipedia.org/wiki/Abbreviated_New_Drug...

    An Abbreviated New Drug Application ( ANDA) is an application for a U.S. generic drug approval for an existing licensed medication or approved drug . The ANDA is submitted to FDA's Center for Drug Evaluation and Research, Office of Generic Drugs, which provides for the review and ultimate approval of a generic drug product.

  3. New Drug Application - Wikipedia

    en.wikipedia.org/wiki/New_Drug_Application

    New Drug Application. The Food and Drug Administration 's (FDA) New Drug Application ( NDA) is the vehicle in the United States through which drug sponsors formally propose that the FDA approve a new pharmaceutical for sale and marketing. [ 1][ 2] Some 30% or less of initial drug candidates proceed through the entire multi-year process of drug ...

  4. Generic top-level domain - Wikipedia

    en.wikipedia.org/wiki/Generic_top-level_domain

    The new generic top-level domain (gTLD) application system opened on January 12, 2012. The application window was initially to close on April 12, 2012. However, ICANN's Chief Operating Officer, Akram Atallah, stated there was a glitch in the TLD application system leaving applicants' information visible to others.

  5. Drug Price Competition and Patent Term Restoration Act

    en.wikipedia.org/wiki/Drug_Price_Competition_and...

    t. e. The Drug Price Competition and Patent Term Restoration Act (Public Law 98-417), informally known as the Hatch-Waxman Act, is a 1984 United States federal law that established the modern system of generic drug regulation in the United States. The Act's two main goals are to facilitate entry of generic drugs into the market and to ...

  6. Authorized generics - Wikipedia

    en.wikipedia.org/wiki/Authorized_generics

    Authorized generics are prescription drugs produced by brand pharmaceutical companies and marketed under a private label, at generic prices. Authorized generics compete with generic products in that they are identical to their brand counterpart in both active and inactive ingredients; whereas according to the U.S. Food and Drug Administration's Office of Generic Drugs, generic drugs are ...

  7. Dosage form - Wikipedia

    en.wikipedia.org/wiki/Dosage_form

    Dosage form. Dosage forms (also called unit doses) are pharmaceutical drug products in the form in which they are marketed for use, with a specific mixture of active ingredients and inactive components ( excipients ), in a particular configuration (such as a capsule shell, for example), and apportioned into a particular dose.