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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

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


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