STEGLUJAN (ERTUGLIFLOZIN AND SITAGLIPTIN)
Summary
FDA approved STEGLUJAN (ERTUGLIFLOZIN AND SITAGLIPTIN) by MSD SUB MERCK. NDA (New Drug) approval (Labeling) on 2026-06-03. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA209805-22
Action Date
2026-06-03
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
STEGLUJAN (generic: ERTUGLIFLOZIN AND SITAGLIPTIN), TABLET, ORAL. Application: NDA209805
Company
Context & Analysis
MSD SUB MERCK has 7 FDA actions in our database.
Frequently Asked Questions
How often does MSD SUB MERCK have FDA actions?
MSD SUB MERCK has 7 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA209805-22" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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