Regulatory · source year

2025 regulatory records

52 selected, source-linked regulatory records dated 2025. This is selective source coverage, not a complete timeline.

Dated records

52 selected records.

Peptide profiles

19 connected profiles.

Cited sources

52 distinct public records.

Cited chronology

Dated source records

Open in the filterable feed →

December 2025

10 records

Elamipretide

Federal Register notice 2025-23409

The Federal Register published notice 2025-23409, attributed to FDA and its parent HHS department, on 2025-12-19. Its official title is “Issuance of Priority Review Voucher; Rare Pediatric Disease Product; FORZINITY (Elamipretide),” and PeptideScanner's exact reviewed identity mapping connects the document to Elamipretide.

Source: Federal Register via GovInfo ↗

Glucagon + 5 more

Federal Register notice 2025-22131

The Federal Register published notice 2025-22131, attributed to FDA and its parent HHS department, on 2025-12-05. Its official title is “Product-Specific Guidances; Draft and Revised Draft Guidances for Industry; Availability,” and PeptideScanner's exact reviewed identity mapping connects the document to Glucagon, Liraglutide, Semaglutide, Teriparatide, Tirzepatide and Vosoritide.

Source: Federal Register via GovInfo ↗

November 2025

8 records

Glucagon + 1 more

Federal Register notice 2025-20548

The Federal Register published notice 2025-20548, attributed to FDA and its parent HHS department, on 2025-11-21. Its official title is “Product-Specific Guidances; Draft and Revised Draft Guidances for Industry; Availability,” and PeptideScanner's exact reviewed identity mapping connects the document to Glucagon and Tirzepatide.

Source: Federal Register via GovInfo ↗

October 2025

2 records

Exenatide + 1 more

Federal Register notice 2025-19281

The Federal Register published notice 2025-19281, attributed to FDA and its parent HHS department, on 2025-10-02. Its official title is “Pediatric Advisory Committee (PAC); Notice of Meeting; Establishment of a Public Docket; Request for Comments,” and PeptideScanner's exact reviewed identity mapping connects the document to Exenatide and Linaclotide.

Source: Federal Register via GovInfo ↗

Semaglutide

Federal Register notice 2025-19345

The Federal Register published notice 2025-19345, attributed to FDA and its parent HHS department, on 2025-10-02. Its official title is “Product-Specific Guidances; Draft and Revised Draft Guidances for Industry; Availability,” and PeptideScanner's exact reviewed identity mapping connects the document to Semaglutide.

Source: Federal Register via GovInfo ↗

September 2025

2 records

August 2025

7 records

Exenatide

Federal Register notice 2025-14683

The Federal Register published notice 2025-14683, attributed to FDA and its parent HHS department, on 2025-08-04. Its official title is “Teva Branded Pharmaceutical Products R&D, Inc., et al.; Withdrawal of Approval of 39 New Drug Applications,” and PeptideScanner's exact reviewed identity mapping connects the document to Exenatide.

Source: Federal Register via GovInfo ↗

July 2025

5 records

June 2025

5 records

May 2025

5 records

April 2025

4 records

March 2025

1 record

February 2025

2 records

January 2025

1 record