eCFR Reference Browser

---

title: "21 CFR §20.116"

source: "https://www.ecfr.gov/current/title-21/section-20.116"

title_number: "21"

volume_number: "1"

chapter_number: "Unknown"

subchapter_code: "A"

subchapter_subject: "GENERAL"

part_code: "20"

part_subject: "PUBLIC INFORMATION"

subpart_code: "F"

subpart_subject: "Availability of Specific Categories of Records"

section_number: "20.116"

section_subject: "Drug and device registration and listing information."

cfr_reference: "21 CFR 20.116"

title_name: "Title 21"

title_subject: "Food and Drugs"

parts_covered: "Parts 1 to 99"

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"

---

Information submitted to the Food and Drug Administration pursuant to section 510(a) through (j) of the Federal Food, Drug, and Cosmetic Act shall be subject only to the special disclosure provisions established in §§ 207.81 and 807.37 of this chapter.

§20.116 - Drug and device registration and listing information.