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

U.S. FDA Requirements: Midodrine Hydrochloride

Pharmaceutical / Drug Definition : Forms active metabolite, desglymidodrine, an alpha1-adrenergic agonist that activates alpha-adrenergic receptors in arteriolar and venous vasculature. This effect increases vascular resistance and ultimately raises blood pressure.

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

Registrar Corp assists Midodrine Hydrochloride companies with:

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