An applicant may ask the Food and Drug Administration to waive any requirement under §§ 201.56 , 201.57 , and 201.80 . A waiver request must be submitted in writing to the Director (or the Director's designee), Center for Drug Evaluation and Research, Food and Drug Administration, Central Document Room, 5901-B Ammendale Rd., Beltsville, MD 20705-1266, or, if applicable, the Director (or the Director's designee), Food and Drug Administration, Center for Biologics Evaluation and Research, Document Control Center, 10903 New Hampshire Ave., Bldg. 71, Rm. G112, Silver Spring, MD 20993-0002. The waiver must be granted or denied in writing by the Director or the Director's designee.
21 CFR Part 201 · Labeling
§ 201.58 Waiver of labeling requirements
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 § 201.58
- Pregnancy, Lactation, and Reproductive Potential: Labeling for Human Prescription Drug and Biological Products-Content and Format: Draft Guidance for Industry draft 29 Jul 2020
- Indications and Usage Section of Labeling for Human Prescription Drug and Biological Products — Content and Format Guidance for Industry draft 6 Jul 2018
- Brief Summary and Adequate Directions for Use: Disclosing Risk Information in Consumer-Directed Print Advertisements and Promotional Labeling for Prescription Drugs draft 6 Aug 2015
- Pregnancy, Lactation, and Reproductive Potential: Labeling for Human Prescription Drug and Biological Products — Content and Format Guidance for Industry (Small Entity Compliance Guide) 10 Jun 2015
- Labeling for Human Prescription Drug and Biological Products - Implementing the PLR Content and Format Requirements 25 Feb 2013
- Adverse Reactions Section of Labeling for Human Prescription Drug and Biological Products — Content and Format 24 Jan 2006
Amendment history
Federal Register documents that created or amended this section.
- 41 FR 6908 13 Feb 1976
- 71 FR 3996 24 Jan 2006
- 74 FR 13112 26 Mar 2009
- 80 FR 18090 3 Apr 2015