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

U.S. FDA Requirements: Phentolamine Mesylate

Pharmaceutical / Drug Definition : Competitively blocks postsynaptic (alpha1) and presynaptic (alpha2) adrenergic receptors. Acts on arterial tree and venous bed, reducing total peripheral resistance and lowering venous return to heart.

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

Registrar Corp assists Phentolamine Mesylate companies with:

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

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U.S. FDA Regulations:

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

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