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

U.S. FDA Requirements: Fenofibrate

Pharmaceutical / Drug Definition : Inhibits triglyceride synthesis in liver, reducing levels of low- and very-low-density lipoproteins. Also increases uric acid secretion.

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

Registrar Corp assists Fenofibrate companies with:

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