Code of Federal Regulations > Title 21 > Chapter I > Part 310 > Subpart D

REGULATIONS

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Regulations last checked for updates: Jun 14, 2025

Title 21 - Food and Drugs last revised: Jun 03, 2025

§ 310.305 - Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications.

§ 310.306 - Notification of a permanent discontinuance or an interruption in manufacturing of marketed prescription drugs for human use without approved new drug applications.

authority: 21 U.S.C. 321,331,351,352,353,355,360b,360j,360hh,361,371,374,375,379e,379k; 42 U.S.C. 216,241,242,262

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