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

U.S. FDA Requirements: Chlorpheniramine Maleate

Pharmaceutical / Drug Definition : Antagonizes effects of histamine at histamine2-receptor sites, preventing histamine-mediated responses

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

Registrar Corp assists Chlorpheniramine Maleate companies with:

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