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

U.S. FDA Requirements: Cimetidine Hydrochloride

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

Registrar Corp assists Cimetidine Hydrochloride companies with:

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