CTP Newsroom
Stay up to date on the latest news and events from FDA's Center for Tobacco Products through the CTP Newsroom.
From press releases to public meetings to email newsletters, stay up to date on the latest news and events from the FDA Center for Tobacco Products.
Latest News
FDA Issues Guidance on Enforcement Priorities for Unauthorized ENDS and Nicotine Pouch Products
Document describes enforcement policies with regard to the marketing of certain ENDS products and nicotine pouch products that do not have premarket authorization
May 8, 2026
CTP Acting Director’s Statement on Application Review
CTP Acting Director Bret Koplow outlines recent developments and upcoming updates related to tobacco product application review
May 7, 2026
FDA Expands Market Access, Authorizes New ENDS Products
This action marks the FDA’s first authorization of non-tobacco and non-menthol ENDS products
May 5, 2026
2026
May
- Meeting Materials Available: PMTA Roundtable on ENDS
- FDA Files MRTP Renewal Applications From 22nd Century Group Inc. and Opens Public Docket
- FDA Issues Guidance on Enforcement Priorities for Unauthorized ENDS and Nicotine Pouch Products
- CTP Acting Director Statement: New Steps Forward in Accelerating Innovation and Efficiency in Product Review
- FDA Expands Market Access, Authorizes New ENDS Products
April
- FDA Issues Not Substantially Equivalent Orders for 28 Cigarette Products
- FDA Adds 18 Constituents to the List of Harmful and Potentially Harmful Constituents, Seeks Comment on Three Additional Constituents
- FDA Renews Authorization for Five IQOS Products to be Marketed with Exposure Modification Claims
- Open Public Comment Period: Draft Guidance on Applications for Flavored E-Cigarettes
February
2025
December
- FDA Announces Roundtable Discussion with Small ENDS Manufacturers on Premarket Application Submissions
- FDA Authorizes 6 Nicotine Pouch Products, Completing Review in Record Time
- FDA Launches Web-Based Tobacco Premarket Application Forms to Enhance Submission Process
November
- Advisory Committee Meeting on MRTP Applications for ZYN Nicotine Pouch Products
- FDA Establishes Closing Date for Public Comments on MRTP Renewal Applications for IQOS Products
October
September
- A Statement From FDA Commissioner Marty Makary, M.D., M.P.H.: Encouraging Retailers to Stop Selling Illegal Vapes
- FDA Launches Program to More Efficiently Review Nicotine Pouch Applications
- HHS, CBP Seize $86.5 Million Worth of Illegal E-Cigarettes in Largest-Ever Operation
August
- FDA Urges Nicotine Pouch Manufacturers To Use Child-Resistant Packaging
- FDA Denies Marketing for blu Disposable E-Cigarette
July
- FDA Seeks Nominations for the Tobacco Products Scientific Advisory Committee – Summer 2025
- Advisory Committee Meeting Scheduled on MRTP Renewal Applications for IQOS Products
- FDA Authorizes Marketing of Tobacco- and Menthol-Flavored JUUL E-Cigarette Products
June
- Modified Risk Applications for ZYN Nicotine Pouches Now Under FDA Scientific Review
- FDA Updates Tobacco Application Forms; Requires Use by July 6
May
March
January
- FDA Authorizes Marketing of 20 ZYN Nicotine Pouch Products After Extensive Scientific Review
- FDA Proposes Significant Step Toward Reducing Nicotine to Minimally or Nonaddictive Level in Cigarettes and Certain Other Combusted Tobacco Products
- A Year in Review: FDA’s Progress on Tobacco Product Regulation in 2024
- Spotlight on Science: Special Feature on the PATH Study
- More Than $7 Million Worth of Illegal E-Cigarettes Seized in Federal Operation
- FDA Issues Final Guidance on Analytical Testing for Industry Use in Tobacco Product Applications
- FDA Updates Import Alerts to Reinforce that All Unauthorized E-Cigarettes May Be Detained Without Physical Examination
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- Press Release Archive (2009 - 2016)
- Email Newsletters & Web Statements Archive (2010 - 2016)
- Features Archive (2013 - 2016)
- Public Meeting and Workshop Archive (2009 - 2016)
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