Title 21

PART 310 SUBPART D

Subpart D - Records and Reports

• 21 U.S.C. 321, 331, 351, 352, 353, 355, 360b-360f, 360j, 360hh-360ss, 361(a), 371, 374, 375, 379e, 379k-l; 42 U.S.C. 216, 241, 242(a), 262.

21:5.0.1.1.2.4.1.1	SECTION 310.305	310.305 Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications.
21:5.0.1.1.2.4.1.2	SECTION 310.306	310.306 Notification of a permanent discontinuance or an interruption in manufacturing of marketed prescription drugs for human use without approved new drug applications.

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