By Dec. 31 of each year, all registered tobacco manufacturers are required to re-register with FDA through TRLM NG module or by paper submission.
Twice each year – by June 30 and Dec. 31 – all registered domestic tobacco manufacturers are required to re-submit their product listings if they have made certain changes.
Learn more about the biannual listing deadline and how FDA is helping you comply.
FDA recommends that you submit your establishment registration and product listings online using the Tobacco Registration and Listing Module – Next Generation (TRLM NG) module.
If you are unable to submit online using TRLM NG, you can mail the appropriate Registration & Listing PDF form (FDA Form 3741) or, for deemed establishments, FDA Form 3741a) to CTP's Document Control Center. See examples of completed registration and listing forms for reference.
Also see the Registration and Product Listing Guidance for more information.
- Guidance: Registration and Product Listing for Owners and Operators of Domestic Tobacco Product Establishments
- Tobacco Registration and Listing Module – Next Generation (TRLM NG)