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

U.S. FDA Requirements: Tromethamine

Pharmaceutical / Drug Definition : Combines with hydrogen ions to form bicarbonate and a buffer, correcting acidosis. Also shows some diuretic activity

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

Registrar Corp assists Tromethamine companies with:

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