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

U.S. FDA Requirements: Scopolamine

Pharmaceutical / Drug Definition : Acts as competitive inhibitor at postganglionic muscarinic receptor sites of parasympathetic nervous system and on smooth muscles that respond to acetylcholine but lack cholinergic innervation. May block cholinergic transmission from vestibular nuclei to higher CNS centers and from reticular formation to vomiting center

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

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


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