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

U.S. FDA Requirements: Epinephrine Bitartrate

Pharmaceutical / Drug Definition : Stimulates alpha- and beta-adrenergic receptors, causing relaxation of cardiac and bronchial smooth muscle and dilation of skeletal muscles. Also decreases aqueous humor production, increases aqueous outflow, and dilates pupils by contracting dilator muscle.

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

Registrar Corp assists Epinephrine Bitartrate companies with:

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