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

U.S. FDA Requirements: Probenecid

Pharmaceutical / Drug Definition : Promotes uric acid excretion from kidney by blocking tubular reabsorption; also inhibits tubular secretion of weak organic acids (most penicillins and cephalosporins, some beta-lactams)

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

Registrar Corp assists Probenecid companies with:

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