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

U.S. FDA Requirements: Sucralfate

Pharmaceutical / Drug Definition : Combines with gastric acid to form protective coating on ulcer surface, inhibiting gastric acid secretion, pepsin, and bile salts

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

Registrar Corp assists Sucralfate companies with:

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