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

U.S. FDA Requirements: Nilutamide

Pharmaceutical / Drug Definition : Inhibits testosterone uptake in target tissue, preventing normal androgenic response and arresting tumor growth in androgen-sensitive tissue

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

Registrar Corp assists Nilutamide companies with:

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