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

U.S. FDA Requirements: Nicotine

Pharmaceutical / Drug Definition : Supplies nicotine during controlled withdrawal from cigarette smoking. Binds selectively to nicotinic-cholinergic receptors in central and peripheral nervous systems, autonomic ganglia, adrenal medulla, and neuromuscular junction. At low doses, has a stimulating effect; at high doses, a reward effect.

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

Registrar Corp assists Nicotine companies with:

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