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

U.S. FDA Requirements: Mesalamine

Pharmaceutical / Drug Definition : Thought to act in colon, where it blocks cyclooxygenase and inhibits prostaglandin synthesis.

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

Registrar Corp assists Mesalamine companies with:

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