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

U.S. FDA Requirements: Nizatidine

Pharmaceutical / Drug Definition : Inhibits histamine action at H2-receptor sites in gastric parietal cells, reducing gastric acid secretion and pepsin production

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

Registrar Corp assists Nizatidine companies with:

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