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

U.S. FDA Requirements: Prazosin Hydrochloride

Pharmaceutical / Drug Definition : Induces peripheral vasodilation by blocking postsynaptic alpha1-adrenergic receptors, thereby lowering blood pressure. Decreases smooth muscle contractions of prostatic capsule and relaxes smooth muscles in bladder neck and prostate.

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

Registrar Corp assists Prazosin Hydrochloride companies with:

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