# Development of Monoclonal Antibody Products Targeting SARS-CoV-2 for Emergency Use Authorization; Guidance for Industry; Correction
**AGENCY:**
Food and Drug Administration, HHS.
**ACTION:**
Correction.
**SUMMARY:**
The Food and Drug Administration (FDA) is correcting a notice that appeared in the *Federal Register* on December 21, 2023. The document announced the availability of a final guidance for industry entitled “Development of Monoclonal Antibody Products Targeting SARS-CoV-2 for Emergency Use Authorization.” The document was published with an incorrect docket number. This document corrects that error.
**FOR FURTHER INFORMATION CONTACT:**
Maria Clary, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 75, Rm. 4638, Silver Spring, MD 20993-0002, 240-402-8615.
**SUPPLEMENTARY INFORMATION:**
In the *Federal Register* of December 21, 2023 (88 FR 88401), in FR Doc. 2023-28092, the following correction is made:
1. On page 88401, in the first column in the header of the document, and in the *ADDRESSES* section, in the second and third lines of the first paragraph, the Docket No. is corrected to read “Docket No. FDA-2024-D-0361.”
Dated: January 25, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.