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

U.S. FDA Requirements: Acetaminophen

Pharmaceutical / Drug Definition : Acetaminophen is used to relieve mild to moderate pain from headaches, muscle aches, menstrual periods, colds, sore throats, toothaches, backaches, reactions to vaccinations (shots), and to reduce fever. Acetaminophen may also be used to relieve the pain of osteoarthritis (arthritis caused by the breakdown of the lining of the joints). Acetaminophen will relieve symptoms but will not treat the cause of symptoms or speed recovery. Acetaminophen is in a class of medications called analgesics (pain relievers) and antipyretics (fever reducers). It works by changing the way the body senses pain and by cooling the body.

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

Registrar Corp assists Acetaminophen companies with:

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