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HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Isosorbide Dinitrate

U.S. FDA Requirements: Isosorbide Dinitrate

Pharmaceutical / Drug Definition : Promotes peripheral vasodilation and reduces preload and afterload, decreasing myocardial oxygen consumption and increasing cardiac output. Also dilates coronary arteries, increasing blood flow and improving collateral circulation.

In the United States, Isosorbide Dinitrate is regulated by the U.S. Food and Drug Administration (FDA). FDA has specific requirements regarding the registration and listing of Isosorbide Dinitrate.

Registrar Corp assists Isosorbide Dinitrate companies with:

  • FDA Registration Isosorbide Dinitrate
  • FDA Listing Isosorbide Dinitrate
  • FDA Label Requirements and Exceptions Isosorbide Dinitrate
  • FDA Import Information Isosorbide Dinitrate
  • FDA Detentions Isosorbide Dinitrate (Isosorbide Dinitrate Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Isosorbide Dinitrate (Isosorbide Dinitrate Suppliers)
       - Processors Isosorbide Dinitrate
       - Repackers Isosorbide Dinitrate
       - Relabelers Isosorbide Dinitrate
       - Exporters Isosorbide Dinitrate
       - Importers Isosorbide Dinitrate
For more information about Isosorbide Dinitrate, simply click below:

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U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207

Registrar Corp assists businesses with U.S. FDA compliance. Certificates of Registration issued by Registrar Corp provide confirmation to industry that you are fulfilling U.S. FDA registration requirements. U.S. FDA does not issue or recognize Certificates of Registration. Registrar Corp is not affiliated with the U.S. Food and Drug Administration.
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