For biological products being considered for approval under this subpart, unless otherwise informed by the agency, applicants must submit to the agency for consideration during the preapproval review period copies of all promotional materials, including promotional labeling as well as advertisements, intended for dissemination or publication within 120 days following marketing approval. After 120 days following marketing approval, unless otherwise informed by the agency, the applicant must submit promotional materials at least 30 days prior to the intended time of initial dissemination of the labeling or initial publication of the advertisement.
21 CFR Part 601 · Licensing
§ 601.45 Promotional materials
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.
FDA guidance that cites § 601.45
- Regulatory Considerations for Prescription Drug Use-Related Software 20 Oct 2026
- Addressing Misinformation About Medical Devices and Prescription Drugs: Questions and Answers draft 8 Jul 2024
- Providing Regulatory Submissions in Electronic and Non-Electronic Format—Promotional Labeling and Advertising Materials for Human Prescription Drugs 11 Apr 2022
Amendment history
Federal Register documents that created or amended this section.
- 38 FR 32052 20 Nov 1973