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

U.S. FDA Requirements: Leuprolide Acetate

Pharmaceutical / Drug Definition : Inhibits and desensitizes GnRH receptors, thus inhibiting gonadotropin secretion when given continuously. This inhibition causes initial increase and then profound decrease in luteinizing hormone and follicle-stimulating hormone levels and, ultimately, reduces testosterone and estrogen sex hormones.

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  • FDA Registration Leuprolide Acetate
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  • FDA Label Requirements and Exceptions Leuprolide Acetate
  • FDA Import Information Leuprolide Acetate
  • FDA Detentions Leuprolide Acetate (Leuprolide Acetate Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Leuprolide Acetate (Leuprolide Acetate Suppliers)
       - Processors Leuprolide Acetate
       - Repackers Leuprolide Acetate
       - Relabelers Leuprolide Acetate
       - Exporters Leuprolide Acetate
       - Importers Leuprolide Acetate
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U.S. FDA Regulations:

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


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