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

U.S. FDA Requirements: Thalidomide

Pharmaceutical / Drug Definition : Suppresses excess levels of tumor necrosis factor-alpha in patients with erythema nodosum leprosum (ENL). Alters leukocyte migration by changing cell surface characteristics.

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

Registrar Corp assists Thalidomide companies with:

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