> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Latest Federal Register Notices
- URL: https://www.fdaweb.com/latest-federal-register-notices-171/
- Published: 2018-03-18T12:00:00.000Z
- Updated: 2026-09-14T23:53:50.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5141012

[**Arthritis Drugs Panel to Review Eli Lilly NDA**](https://www.fdaweb.com/arthritis-drugs-panel-to-review-eli-lilly-nda/)  
*Federal Register* notice: FDA announces a 4/23 Arthritis Advisory Committee meeting that will review an Eli Lilly NDA for baricitinib tablets. 03/16/2018

[**Comments Sought on MedWatch Info Collection**](https://www.fdaweb.com/comments-sought-on-medwatch-info-collection/)  
*Federal Register* notice: FDA seeks comments on an information collection extension for “MedWatch: The FDA Medical Products Reporting Program” (OMB Control Number 0910-0291). 03/16/2018

[**Joint Advisory Panel Discussing Achondroplasia Amended**](https://www.fdaweb.com/joint-advisory-panel-discussing-achondroplasia-amended/)  
*Federal Register* notice: FDA amends a 1/23 notice about a 3/22 Pediatric Advisory Committee and Endocrinologic and Metabolic Drugs Advisory Committee meeting to reflect a change in the agenda. 03/16/2018

[**Comments Sought on Professional Rx Promotion**](https://www.fdaweb.com/comments-sought-on-professional-rx-promotion/)  
*Federal Register* notice: FDA seeks comments on a proposed collection of information — “Health Care Professional Survey of Professional Prescription Drug Promotion.” 03/15/2018

[**FDA Exempts OTC Denture Repair Kits**](https://www.fdaweb.com/fda-exempts-otc-denture-repair-kits/)  
*Federal Register* notice: FDA issues an order exempting from premarket notification (510(k) requirements over-the-counter denture repair kits. 03/15/2018

[**Lynch Syndrome Test Classification Notice Corrected**](https://www.fdaweb.com/lynch-syndrome-test-classification-notice-corrected/)  
*Federal Register* correction notice: FDA corrects a final order entitled “Medical Devices; Hematology and Pathology Devices; Classification of Lynch Syndrome Test Systems. 3/14/2018

[**4 Sun Pharma ANDA Approvals Withdrawn**](https://www.fdaweb.com/4-sun-pharma-anda-approvals-withdrawn/)  
*Federal Register* notice: FDA withdraws approval of four Sun Pharmaceutical ANDAs because the drug products are no longer marketed. 03/14/2018

[**Meeting on Opioid Use Disorder Drugs**](https://www.fdaweb.com/meeting-on-opioid-use-disorder-drugs/)  
*Federal Register* notice: FDA announces a 4/17 public meeting entitled “Patient-Focused Drug Development on Opioid Use Disorder.” 03/14/2018