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

U.S. FDA Requirements: Acitretin

Pharmaceutical / Drug Definition : Promotes normal growth cycle of skin cells, possibly by targeting retinoid receptors in these cells and adjusting factors that affect epidermal proliferation and synthesis of RNA and DNA.

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

Registrar Corp assists Acitretin companies with:

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