Health and Human Services Department, Food and Drug Administration
The Food and Drug Administration (FDA or the Agency) is extending the comment period for the proposed rule entitled "Requirements for Tobacco Product Manufacturing Practice" published in the Federal Register of March 10, 2023, by 30 days. The Agency is taking this action in response to a request for an extension to allow interested persons additional time to submit comments.
Document Headings Document headings vary by document type but may contain the following: the agency or agencies that issued and signed a document the number of the CFR title and the number of each part the document amends, proposes to amend, or is directly related to the agency docket number / agency internal file number the RIN which identifies each regulatory action listed in the Unified Agenda of Federal Regulatory and Deregulatory Actions See the Document Drafting Handbook for more details. Department of Health and Human Services Food and Drug Administration 21 CFR Part 1120 [Docket No. FDA-2013-N-0227] RIN 0910-AH91 AGENCY: Food and Drug Administration, HHS. ACTION: Proposed rule; extension of comment period. SUMMARY: The Food and Drug Administration (FDA or the Agency) is extending the comment period for the proposed rule entitled “Requirements for Tobacco Product Manufacturing Practice” published in the Federal Register of March 10, 2023, by 30 days. The Agency is taking this action in response to a request for an extension to allow interested persons additional time to submit comments. DATES: FDA is extending the comment period on the proposed rule published March 10, 2023 ( 88 FR 15174 ), by 30 days. Either electronic or written comments must be submitted by October 6, 2023. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. The https://www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of October 6, 2023. Comments received by mail/hand delivery/courier (for written/paper submissions) will be considered timely if they are received on or before that date. Electronic Submissions Submit electronic comments in the following way: Federal eRulemaking Portal: https://www.regulations.gov . Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to https://www.regulations.gov will be…
Other Federal Register documents from the same docket.
Proposed Requirements for Tobacco Products Manufacturing Practice; Tobacco Products Scientific Advisory Committee; Notice of Meeting; Request for Comments
Proposed Requirements for Tobacco Product Manufacturing Practice; Public Hearing; Request for Comments
Requirements for Tobacco Product Manufacturing Practice
Tobacco Product Manufacturing Practice; Request for Comments
Tobacco Product Manufacturing Practice; Establishment of a Public Docket
Citation: 88 FR 59481