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HomeDrugsU.S. FDA Active Pharmaceutical Ingredients (API)API Examples › U.S. FDA Regulations: Bromocriptine Mesylate

U.S. FDA Requirements: Bromocriptine Mesylate

Pharmaceutical / Drug Definition : Directly stimulates dopamine receptors in hypothalamus, causing release of prolactin-inhibitory factors and thereby relieving akinesia, rigidity, and tremors associated with Parkinson's disease. Also restores testicular or ovarian function and suppresses lactation.

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

Registrar Corp assists Bromocriptine Mesylate companies with:

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