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

U.S. FDA Requirements: Ceftazidime

Pharmaceutical / Drug Definition : Interferes with bacterial cell-wall synthesis and division by binding to cell wall, causing cell to die. Active against gram-negative and gram-positive bacteria, with expanded activity against gram-negative bacteria. Exhibits minimal immunosuppressant activity.

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

Registrar Corp assists Ceftazidime companies with:

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