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

U.S. FDA Requirements: Quinine Sulfate

Pharmaceutical / Drug Definition : Thought to interfere with DNA synthesis by increasing pH in intracellular organelles of susceptible parasites.

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

Registrar Corp assists Quinine Sulfate companies with:

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