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

U.S. FDA Requirements: Zidovudine

Pharmaceutical / Drug Definition : After conversion to its active metabolite, inhibits activity of HIV reverse transcriptase and terminates viral DNA growth

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

Registrar Corp assists Zidovudine companies with:

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