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

U.S. FDA Requirements: Azathioprine

Pharmaceutical / Drug Definition : Prevents proliferation and differentiation of activated B and T cells by interfering with synthesis of purine, DNA, and RNA

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

Registrar Corp assists Azathioprine companies with:

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