eCFR Reference Browser

---

title: "21 CFR §1301.01"

source: "https://www.ecfr.gov/current/title-21/section-1301.01"

title_number: "21"

volume_number: "9"

chapter_number: "Unknown"

subchapter_code: "Unknown"

subchapter_subject: "Unknown"

part_code: "1301"

part_subject: "REGISTRATION OF MANUFACTURERS, DISTRIBUTORS, AND DISPENSERS OF CONTROLLED SUBSTANCES"

subpart_code: "A"

subpart_subject: "General Requirements"

section_number: "1301.01"

section_subject: "Scope of this part 1301."

cfr_reference: "21 CFR 1301.01"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Part 1300 to End"

revised_date: "Revised as of April 1, 2019"

publication_date: "As of April 1, 2019"

contains_description: "Containing a codification of documents of general applicability and future effect"

publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"

---

Procedures governing the registration of manufacturers, distributors, dispensers, importers, and exporters of controlled substances pursuant to sections 301-304 and 1007-1008 of the Act (21 U.S.C. 821-824 and 957-958) are set forth generally by those sections and specifically by the sections of this part.

§1301.01 - Scope of this part 1301.