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

U.S. FDA Requirements: Clomipramine Hydrochloride

Pharmaceutical / Drug Definition : Selectively inhibits norepinephrine and serotonin reuptake at presynaptic neurons in brain; also possesses moderate anticholinergic properties.

Registrar Corp assists Clomipramine Hydrochloride companies with:

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