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

U.S. FDA Requirements: Calcium Chloride

Pharmaceutical / Drug Definition : Increases serum calcium level through direct effects on bone, kidney, and GI tract. Decreases osteoclastic osteolysis by reducing mineral release and collagen breakdown in bone.

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

Registrar Corp assists Calcium Chloride companies with:

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