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

U.S. FDA Requirements: Zonisamide

Pharmaceutical / Drug Definition : Raises seizure threshold and reduces seizure duration, probably by stabilizing neuronal membranes through action on sodium and calcium channels.

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

Registrar Corp assists Zonisamide companies with:

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