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

U.S. FDA Requirements: Magnesium Sulfate

Pharmaceutical / Drug Definition : Increases osmotic gradient in small intestine, which draws water into intestines and causes distention. These effects stimulate peristalsis and bowel evacuation. In antacid action, reacts with hydrochloric acid in stomach to form water and increase gastric pH. In anticonvulsant action, depresses CNS and blocks transmission of peripheral neuromuscular impulses.

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

Registrar Corp assists Magnesium Sulfate companies with:

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