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

U.S. FDA Requirements: Albuterol

Pharmaceutical / Drug Definition : Relaxes smooth muscles by stimulating beta2-receptors, thereby causing bronchodilation and vasodilation

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

Registrar Corp assists Albuterol companies with:

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