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

U.S. FDA Requirements: Temazepam

Pharmaceutical / Drug Definition : Depresses CNS at limbic, thalamic, and hypothalamic levels. Enhances effects of gamma-aminobutyric acid, resulting in sedation, hypnosis, skeletal muscle relaxation, and anticonvulsant and anxiolytic activity

Registrar Corp assists Temazepam companies with:

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