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

U.S. FDA Requirements: Sildenafil Citrate

Pharmaceutical / Drug Definition : Inhibits PDE5, enhancing the effects of nitric oxide released during sexual stimulation. This action inactivates cyclic guanosine monophosphate (cGMP), which then increases cGMP levels in corpus cavernosum. Resulting smooth muscle relaxation promotes increased blood flow and subsequent erection

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  • FDA Detentions Sildenafil Citrate (Sildenafil Citrate Entry Refusal)
  • General U.S. Food and Drug Administration Guidelines for:
       - Manufacturers Sildenafil Citrate (Sildenafil Citrate Suppliers)
       - Processors Sildenafil Citrate
       - Repackers Sildenafil Citrate
       - Relabelers Sildenafil Citrate
       - Exporters Sildenafil Citrate
       - Importers Sildenafil Citrate
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U.S. FDA Regulations:

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


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