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

U.S. FDA Requirements: Fluoxetine Hydrochloride

Pharmaceutical / Drug Definition : Selectively inhibits serotonin reuptake in CNS; has little to no effect on norepinephrine and dopamine reuptake

Registrar Corp assists Fluoxetine Hydrochloride companies with:

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