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

U.S. FDA Requirements: Lanthanum Carbonate

Pharmaceutical / Drug Definition : Dissociates in acidic environment of upper GI tract to release lanthanum ions, which bind dietary phosphate released from food during digestion and inhibit phosphate absorption by forming highly insoluble lanthanum phosphate complexes

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

Registrar Corp assists Lanthanum Carbonate companies with:

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