2017-24948. Controlled Correspondence Related to Generic Drug Development; Draft Guidance for Industry; Availability; Correction
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Start Preamble
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice; correction.
SUMMARY:
The Food and Drug Administration is correcting a notice entitled “Controlled Correspondence Related to Generic Drug Development; Draft Guidance for Industry; Availability” that appeared in the Start Printed Page 54387 Federal Register of November 3, 2017. The document announced the availability of a draft guidance for industry. The document was published with the incorrect docket number. This document corrects that error.
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Lisa Granger, Office of Policy, Food and Drug Administration, 10903 New Hampshire Ave. Bldg. 32, Rm. 3330, Silver Spring, MD 20993-0002, 301-796-9115, lisa.granger@fda.hhs.gov.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
In the Federal Register of Friday, November 3, 2017 (82 FR 51277), in FR Doc. 2017-23947, the following correction is made:
On page 51277, in the second column, in the header of the document, “[Docket FDA-2014-D-1147]” is corrected to read “[Docket No. FDA-2014-D-1167]”.
Start SignatureDated: November 9, 2017.
Anna K. Abram,
Deputy Commissioner for Policy, Planning, Legislation, and Analysis.
[FR Doc. 2017-24948 Filed 11-16-17; 8:45 am]
BILLING CODE 4164-01-P
Document Information
- Published:
- 11/17/2017
- Department:
- Food and Drug Administration
- Entry Type:
- Notice
- Action:
- Notice; correction.
- Document Number:
- 2017-24948
- Pages:
- 54386-54387 (2 pages)
- Docket Numbers:
- Docket No. FDA-2014-D-1167
- PDF File:
- 2017-24948.pdf
- Supporting Documents:
- » Controlled Correspondence Related to Generic Drug Development; Guidance for Industry
- » Controlled Correspondence Related to Generic Drug Development; Guidance for Industry; Availability
- » Controlled Correspondence Related to Generic Drug Development; Draft Guidance for Industry; Availability; Correction
- » Draft Guidance for Industry on Controlled Correspondence Related to Generic Drug Development
- » Controlled Correspondence Related to Generic Drug Development; Draft Guidance for Industry; Availability
- » Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Guidance for Industry on Controlled Correspondence Related to Generic Drug Development
- » Controlled Correspondence Related to Generic Drug Development Guidance for Industry
- » Controlled Correspondence Related to Generic Drug Development; Guidance for Industry; Availability
- » Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Guidance for Industry on Controlled Correspondence Related to Generic Drug Development
- » Draft Guidance for Industry on Controlled Correspondence Related to Generic Drug Development