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

U.S. FDA Requirements: Triptorelin Pamoate

Pharmaceutical / Drug Definition : Initially causes surge in luteinizing hormone (LH), follicle-stimulating hormone (FSH), and testosterone levels. After several weeks of therapy, LH and FSH secretion decrease, causing sustained testosterone reduction equivalent to pharmacologic castration

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




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U.S. FDA Regulations:

U.S. FDA Regulation: 21 C.F.R. Part 207


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