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

U.S. FDA Requirements: Cimetidine

Pharmaceutical / Drug Definition : Competitively inhibits histamine action at histamine2-receptor sites of gastric parietal cells, thereby inhibiting gastric acid secretion

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

Registrar Corp assists Cimetidine companies with:

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