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

U.S. FDA Requirements: Citalopram Hydrobromide

Pharmaceutical / Drug Definition : Thought to potentiate serotonergic activity in CNS by inhibiting neuronal uptake of serotonin.

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

Registrar Corp assists Citalopram Hydrobromide companies with:

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