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

U.S. FDA Requirements: Pseudoephedrine Sulfate

Pharmaceutical / Drug Definition : Stimulates alpha-adrenergic receptors, causing vasoconstriction of respiratory tract; relaxes bronchial smooth muscle through beta2-adrenergic stimulation

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

Registrar Corp assists Pseudoephedrine Sulfate companies with:

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