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

U.S. FDA Requirements: Chloroquine Phosphate

Pharmaceutical / Drug Definition : Antimalarial action may occur through inhibition of protein synthesis and alteration of DNA in susceptible parasites.

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

Registrar Corp assists Chloroquine Phosphate companies with:

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