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List of Drug Products That Have Been Withdrawn or Removed From the Market for Reasons of Safety or Effectiveness
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The Food and Drug Administration (FDA) is proposing to amend its regulations to include a list of drug products that may not be used for pharmacy compounding pursuant to the exemptions under section 503A of the Federal Food, Drug, and Cosmetic Act (the act) because they have had their approval withdrawn or were removed from the market because the drug product or its components have been found to be unsafe or not effective. The list has been compiled under the new statutory requirements of the Food and Drug Administration Modernization Act of 1997 (Modernization Act).
Oorspronkelijke brontaal: Federal Register — Food and Drug AdministrationOrigineel bericht openen →