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

U.S. FDA Requirements: Colesevelam Hydrochloride

Pharmaceutical / Drug Definition : Binds bile acids in GI tract and forms insoluble complex, impeding bile acid reabsorption and promoting its excretion. As a result, cholesterol and low-density lipoprotein (LDL) levels decrease.

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

Registrar Corp assists Colesevelam Hydrochloride companies with:

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