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

U.S. FDA Requirements: Epinephrine

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

Registrar Corp assists Epinephrine companies with:

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