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

U.S. FDA Requirements: Dipyridamole

Pharmaceutical / Drug Definition : Interferes with histamine effects at histamine1-receptor sites; prevents but doesn't reverse histamine-mediated response. Also possesses CNS depressant and anticholinergic properties.

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

Registrar Corp assists Dipyridamole companies with:

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