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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.

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
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U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207


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