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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 207 - PART 207—REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTABLISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, INCLUDING DRUGS THAT ARE REGULATED UNDER A BIOLOGICS LICENSE APPLICATION, AND ANIMAL DRUGS, AND THE NATIONAL DRUG CODE
  • Subpart A [§ 207.1 - § 207.13] - Subpart A—General
  • Subpart B [§ 207.17 - § 207.29] - Subpart B—Registration
  • Subpart C [§ 207.33 - § 207.37] - Subpart C—National Drug Code
  • Subpart D [§ 207.41 - § 207.57] - Subpart D—Listing
  • Subpart E [§ 207.61 - § 207.65] - Subpart E—Electronic Format for Registration and Listing
  • Subpart F [§ 207.69 - § 207.81] - Subpart F—Miscellaneous
authority: 21 U.S.C. 321,331,351,352,355,360,360b,371,374,381,393; 42 U.S.C. 262,264,271
source: 81 FR 60212, Aug. 31, 2016, unless otherwise noted.
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