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

U.S. FDA Requirements: Promethazine Hydrochloride

Pharmaceutical / Drug Definition : Blocks effects but not release of histamine and exerts strong alpha-adrenergic effect. Also inhibits chemoreceptor trigger zone in medulla and alters dopamine effects by indirectly reducing reticular stimulation in CNS.

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

Registrar Corp assists Promethazine Hydrochloride companies with:

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