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

U.S. FDA Requirements: Theophylline

Pharmaceutical / Drug Definition : Relaxes bronchial smooth muscles, suppressing airway response to stimuli. Also inhibits phosphodiesterase and release of slow-reacting substance of anaphylaxis and histamine

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

Registrar Corp assists Theophylline companies with:

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