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

U.S. FDA Requirements: Phenytoin Sodium

Pharmaceutical / Drug Definition : Thought to limit seizure activity by promoting sodium efflux from neurons in motor cortex and reducing activity in brainstem centers responsible for tonic phase of tonic-clonic seizures

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

Registrar Corp assists Phenytoin Sodium companies with:

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