GLYXAMBI (EMPAGLIFLOZIN AND LINAGLIPTIN)
Summary
FDA approved GLYXAMBI (EMPAGLIFLOZIN AND LINAGLIPTIN) by BOEHRINGER INGELHEIM. NDA (New Drug) approval (Labeling) on 2025-10-24. TABLET, ORAL.
Details
Source
Drug Approval
External ID
NDA206073-44
Action Date
2025-10-24
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
GLYXAMBI (generic: EMPAGLIFLOZIN AND LINAGLIPTIN), TABLET, ORAL. Application: NDA206073
Company
Context & Analysis
BOEHRINGER INGELHEIM has 10 FDA actions in our database.
Frequently Asked Questions
How often does BOEHRINGER INGELHEIM have FDA actions?
BOEHRINGER INGELHEIM has 10 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 "NDA206073-44" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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