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

U.S. FDA Requirements: Leflunomide

Pharmaceutical / Drug Definition : Inhibits T-cell pyrimidine biosynthesis, tyrosine kinases, and dihydroorotate dehydrogenase, blocking structural damage caused by inflammatory response to autoimmune process. Also shows analgesic, antipyretic, and histamine-blocking activity.

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

Registrar Corp assists Leflunomide companies with:

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