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

U.S. FDA Requirements: Olsalazine Sodium

Pharmaceutical / Drug Definition : Converts to active form, mesalamine, which blocks cyclooxygenase and inhibits prostaglandin production in colon.

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

Registrar Corp assists Olsalazine Sodium companies with:

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