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

U.S. FDA Requirements: Inamrinone Lactate

Pharmaceutical / Drug Definition : Inhibits cyclic adenosine monophosphate (cAMP) phosphodiesterase activity in myocardium, increasing cellular levels of cAMP (which regulates intracellular and extracellular calcium levels). These actions increase myocardial contraction force. Also relaxes and dilates vascular smooth muscle, decreasing preload and afterload.

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

Registrar Corp assists Inamrinone Lactate companies with:

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