21 CFR Part 314 · Applications for FDA Approval to Market a New Drug

§ 314.104 Drugs with potential for abuse

Subpart D - FDA Action on Applications and Abbreviated Applications Official text on eCFR Amendment history

The Food and Drug Administration will inform the Drug Enforcement Administration under section 201(f) of the Controlled Substances Act ( 21 U.S.C. 801 ) when an application or abbreviated application is submitted for a drug that appears to have an abuse potential.

Independent copy, not an official legal edition. 21 CFR is a U.S. Government work in the public domain; this text comes from the eCFR and the annual CFR edition, and may lag recent amendments. The authoritative version is on ecfr.gov. Compliome is not affiliated with or endorsed by FDA. Not legal advice.

Amendment history

Federal Register documents that created or amended this section.