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

U.S. FDA Requirements: Telithromycin

Pharmaceutical / Drug Definition : Blocks protein synthesis by binding to domains II and V of 23S rRNA of 50S ribosomal subunit. Binding at domain II enables drug to retain activity against gram-positive cocci in resistance mediated by methylases that alter domain-V binding site

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

Registrar Corp assists Telithromycin companies with:

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