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

U.S. FDA Requirements: Mifepristone

Pharmaceutical / Drug Definition : Antagonizes progesterone receptor sites, inhibiting activity of endogenous and exogenous progesterone and stimulating uterine contractions, which causes fetus to separate from placental wall

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

Registrar Corp assists Mifepristone companies with:

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