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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.

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


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