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

U.S. FDA Requirements: Mirtazapine

Pharmaceutical / Drug Definition : Potentiates effects of norepinephrine and serotonin by blocking their synaptic reuptake. Also exerts anticholinergic activity by disrupting muscarinic receptors.

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

Registrar Corp assists Mirtazapine companies with:

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