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

U.S. FDA Requirements: Zalcitabine

Pharmaceutical / Drug Definition : converted by cellular enzymes to active drug; functions as antimetabolite to inhibit replication of HIV in vitro

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

Registrar Corp assists Zalcitabine companies with:

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